Methods for generating resistance against cgmmv in plants

ABSTRACT

The present invention relates to methods for generating resistance against Cucumber Green Mottle Mosaic Virus (CGMMV) in plants, in particular in plants susceptible to infection by CGMMV, such as  Cucurbitaceae  species, including melon, cucumber, watermelon and bottlegourd. The methods are based on the use of genetic constructs that induce post-transcriptional gene silencing and/or use a nucleotide sequence that encodes a defective variant of the replicase of CGMMV.

[0001] The present invention rates to a method for generating resistance against Cucumber Green Mottle Mosaic Vim (CGMMV) in plus, in particular in plants that are susceptible to infection by CGMMV, such as species of the Cucurbitaceae family.

[0002] The invention further relates to genetic constructs suitable or use in said method, and to CGMMV-resistant transgenic plants obtained via said method.

[0003] Methods of introducing DNA sequences into the genome of plants have been known for many years and have been widely used to alter the properties of plants varieties. Such methods are among others Agrobacterium-mediated transformation (Horsch et al., 1985; Rogers et al., 1986), protoplast transformation using electroporation or other techniques to introduce naked DNA molecules into the plant call (Shillito et al. 1985), and particle bombardment to introduce naked DNA molecules into plant cells or tissues (Christou et al., 1994).

[0004] Among the most important applications of plant genetic engineering are those aimed at introducing resistance genes to a wide variety of plant pests and plant pathogens, such as bacteria, fungi, nematodes, insects and viruses. Many examples of virus resistance in a wide variety of plant species have been described over the last decades (Wilson et al., 1993). The various methods to obtain virus resistance in plants through the introduction of gene sequences are either based on the use of genes of plant origin; on the use of sequences/genes derived from the viral pathogen itself (so-called pathogen-derived resistance (Wilson et al., 1993), or on the use of genes of yet different origin. Sequences originating from the viral genome can be either cloned or PCR-amplified DNA sequences obtain from the genome of DNA viruses, such as geminiviruses (Kunik et al., 1994) or the cDNA sequences obtained from the genomes of RNA viruses through the use of cDNA cloning or RT-PCR amplification.

[0005] Examples of sequences/genes of RNA viruses that have been successfully used in the engine of virus resistance in plants include:

[0006] 1. cost protein genes of tobamoviruses, cucumoviruses, potyviruses, potexviruses (Beachy et al., 1990);

[0007] 2. RNA dependent RNA polymerase genes (replicase genes) of tobamoviruses, cucumoviruses, potyviruses (Anderson et al., 1992; Donson et al., 1993; Audy et al., 1994);

[0008] 3. nucleoprotein genes of tospoviruses (Goldbach and De Haan, 1993; Prins et al., 1994; Vaira et al., 1995);

[0009] 4. movement protein genes of tobamoviruses and cucumviruses (Cooper et al, 1995).

[0010] Cucumber Green Mottle Mosaic Virus (CGMMV) is a member of the tobamovirus group and infects plant species of the Cucurbitaceae family: melon (Cucumis melo), cucumber (C. sativus), watermelon (Citrullus vulgaris) and bottlegourd (Lagenaria siceraria), but not apparently Cucurbita pepo (squash, pumpkin, courgette). The host range of the virus is basically restricted to members of the Cucurbitaceae and/or the diagnostic species Datura stramonium and Chenopodium amaranticolor (Hollings et al., 1975).

[0011] Several different strains can be distinguished seriologically and by their response in C. amaranticolor and D. stramonium (Hollings et al., 1975) The “type strain” was originally identified in Europe and does not normally cause fruit symptoms in cucumber. Another European strain, called the cucumber aucuba mosaic strain, cucumber virus 4 or Cucumis virus 2A causes fruit symptoms in cucumber. A number of strains are known from Japan. In watermelon, the watermelon strain causes serious disease, whereas the Japanese cucumber strain (also called Kyuri Green Mottle Mosaic Virus) and the Yodo strain cause fruit distortions in cucumber. The CGMMV-C strain from India is a pathogen on bottlegourd and serious infectious can cause complete crop losses.

[0012] In cucumber, CGMMV causes vein clearing light and dark green leaf mottle, leaf blistering and malformation and stunted growth, seriously affecting fruit yield. The East European isolates of the aucuba mosaic strain produces bright yellow leaf mottling and fruit discoloration.

[0013] CGMMV is transmitted through seed, but mostly through mechanical infection via the roots in contaminated soil, and through foliage contact and handing of plants (Hollings et al., 1975). The virus particles are extremely stable and survive several months at normal temperatures. This stability combined with the very high infectivity through mechanical contact of the foliage is responsible for the economic importance of this virus as even one or a few infected plants in a cucumber greenhouse can eventually cause the infection and loss of the total crop. Also, infection may not only spread rapidly over a current crop, but also—due to the strong persistance of the virus—affect subsequent crops. Therefore, a CGMMV infection may require sterilization of an anti greenhouse, as well as the use of sterile tools and materials.

[0014] The complete sequence of only one isolate of CGMMV has been determined (Ugaki et al., 1991; Genbank accession numbers D12505 and D01188). This isolate “SH” had been found in infected watermelon plants in East Asia. Furthermore, the sequence of the coat protein gene of one other isolate (“W”) obtained from infected watermelon is known (Meshi et al., 1983; Genbank accession numbers V01551 and J02054), as well as the sequence of the 29 kD movement protein gene of a watermelon strain (Saito et al., 1988; Genbank accession number J04332). The nucleotide sequence of the CGMMV-SH isolate shows 55 to 56% identity with tobacco mosaic virus (TMV) and tobacco mild green mosaic (TMGMV), both other members of the tobamovirus group (Ugaki et al., 1991).

[0015] As described by Ugaki et al., the genome of CGMMV consists of a single-stranded RNA molecule coding for at least four open reading frames, encoding putative proteins of 186 kD, 129 kD, 29 kD and 17.3 kD, of which the 17.3 kD ORF is known to encode the coat protein. In this respect, Ugaki et al. state “No CGMMV-encoded proteins except for the coat protein have yet been identified in vivo”.

[0016] The CGMMV genome is schematically shown in FIG. 1. As can be seen therein, the ORF encoding the 186 kD protein starts at the same site as the ORF encoding the 129 kD) protein, and adds a putative 57 kD polypeptide to the 129 kD ORF. The presence of this 57 kD protein alone has not been detected in infected plants. Instead, the 186 kD protein has been found, being the product of a read-through translation of the 129 kD and the 57 kD ORFs.

[0017] This 186 kD protein is thought to play a role in virus replication. Also, the 129 kD ORF is thought to encode a replicase function, whereas the 29 kD ORF is thought to encode a movement protein.

[0018] Hereinbelow, the nucleotide sequence corresponding to the ORF encoding the 129 kD protein will be referred to as “129 kDs sequence”, the sequence corresponding to the 186 kD readthrough protein will be referred to as “186 kD sequence”, and the nucleotide sequence corresponding to the ORF encoding the 57 kD readthrough part will be referred to as “57 kD sequence”. These nucleotide sequences and the corresponding protein sequences are given in the sequence listings, as further described below.

[0019] Object of the invention was to provide a method for protecting plants, in particular plants susceptible to infection with CGMMV such as species of the Cucurbitaceae family, against infection with CGMMV, and in particular against infection with strains of CGMMV prevalent in Europe, such as the strains encountered in the cultivation of cucumbers in greenhouses.

[0020] Further objects were to provide means for use in said method, in particular a genetic construct that can be used for transforming plants or plant material so as to provide transgenic plants resistant against infection with CGMMV. Further objects of the invention will become clear from the description given hereinbelow.

[0021] For these purposes, applicant has investigated the symptomatology and the nucleotide sequence of the coat protein genes of 10 European strains of CGMMV, and compared these with the SH strain described by Ugaki et al. A list of these strains, with their geographical origin and symptoms on cucumber, is given in Table 1. TABLE 1 List of collected CGMMV-isolates with their geographical origin and symptoms on cucumber. CGMMV isolate Geographical origin Symptoms on cucumber  1 Eastern Europe vein clearing, mosaic  2 Eastern Europe vein clearing, mosaic  3 IPO-DLO, the Netherlands almost without symptoms  4 The Netherlands weak leaf chlorosis  5 The Netherlands weak leaf chlorosis  6 Proefstation Naaldwijk, Chlorosis the Netherlands  7 Rijk Zwaan, the Netherlands Chlorosis  8 Israel Chlorosis  9 Almeria, Spain chlorotic leaf spots 10 Almeria, Spain weak leaf chlorosis CGMMV-SH Japan strong chlorotic leaf mosaic

[0022] It was found that the sequences for the 10 European isolates are highly homologous (i.e. homology on the nucleotide level of 97%), and show about 90% homology (on the nucleotide level) with the SH-isolate. The nucleotide sequences encoding the coat proteins of each of the isolates 1-10, as well as strain SH, are given in the sequence listings, as further described below. The corresponding phytogenetic tree is shown in FIG. 2. This shows that the European isolates can be considered to constitute a subgroup of the CGMMV species.

[0023] In the sequence listings:

[0024] SEQ ID no.1 gives the nucleotide sequence encoding the 129 kD replicase protein of CGMMV isolate 4, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0025] SEQ ID no.2 gives the amino acid sequence of the 129 kD replicase protein of CGMMV isolate 4; with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0026] SEQ ID no.3 gives the nucleotide sequence encoding the 57 kD protein of CGMMV isolate 4, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0027] SEQ ID no.4 gives the amino acid sequence of the 57 kD replicase protein of CGMMV isolate 4, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0028] SEQ ID no.5 gives the nucleotide sequence encoding the 186 kD readthrough protein of CGMMV isolate 4, with the ORF of the coat protein staring with the ATG codon at bp 523-525;

[0029] SEQ ID no.6 gives the amino acid sequence of the 186 kD readthrough protein of CGMMV isolate 4, with the ORF of the coat protein staring with the ATG codon at bp 523-525;

[0030] SEQ ID no.7 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 1, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0031] SEQ ID no.8 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 2, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0032] SEQ ID no.9 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 3, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0033] SEQ ID no.10 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 4, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0034] SEQ ID no.11 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 5, with the ORF of the coat protein stating with the ATG codon at bp 523-525;

[0035] SEQ ID no.12 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 6, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0036] SEQ ID no.13 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 7, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0037] SEQ ID no.14 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 8, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0038] SEQ ID no.15 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 9, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0039] SEQ ID no.16 gives the nucleotide sequence encoding the coat protein of CGMMV isolate 10, with the ORF of the coat protein starting with the ATG codon at bp 523-525;

[0040] SEQ ID no.17 gives the nucleotide sequence encoding the 129 kD replicase protein of CGMMV isolate SH;

[0041] SEQ ID no.18 gives the amino acid sequence of the 129 kD replicase protein of CGMMV isolate SH;

[0042] SEQ ID no. 19 gives the nucleotide sequence encoding the 57 kD protein of CGMMV isolate SH;

[0043] SEQ ID no.20 gives tie amino acid sequence of the 57 kD replicase protein of CGMMV isolate SH,

[0044] SEQ ID no.21 gives the nucleotide sequence encoding the 186 kD readthrough protein of CGMMV isolate SH;

[0045] SEQ ID no.22 gives the amino acid sequence of the 186 kD readthrough protein of CGMMV isolate SH;

[0046] SEQ ID no.23 gives the nucleotide sequence encoding the coat protein of CGMMV isolate SH;

[0047] SEQ ID's nos. 24-40 give the nucleotide sequences of the primers used in the Examples;

[0048] SEQ ID's nos. 41-44 give the nucleotide sequences used in assembling the leader sequences used in the constructs described in the Examples;

[0049] In the above sequence listings, the nucleotide sequences given are DNA sequences, as the genetic constructs of the invention described below will usually contain or consist of a DNA. As CGMMV is an RNA virus, it will be clear to the skilled person that these sequences will occur in the virus as the corresponding RNA sequence (i.e. with U replacing T). Also, it will be clear to the skilled person th the nucleotide sequences given above may be followed—both in the virus as well as in a construct of the invention—with a suitable termination codon, i.e. TAA/UAA, TAG/UAG or TGA/UGA (not shown).

[0050] Furthermore, as will be clear to the skilled person, the nucleotide sequence encoding the coat protein win usually start with an ATG codon. For example, in SEQ ID NOs 1-16, the nucleotide sequence encoding the coat protein starts at the ATG codon at base positions 523-525. (In the nucleotide sequence of SEQ ID NOs 1-16, the nucleotide sequence encoding the coat protein is preceded by another nucleotide sequence, e.g. encoding a movement protein. Accordingly, when hereinbelow reference is made to any nucleotide sequence of SEQ ID NOs 1-16, this also explicitly includes the nucleotide sequence starting at the ATG codon at base positions 523-525 of these SEQ ID's).

[0051] A particular purpose of the invention is therefore to provide a method that can provide plants with resistance against all the strains simultaneously, and more in particular a type of resistance that is agronomically useful, i.e. that can be used to generate a resistance of an extreme nature and/or that can be used to protect (crops of) plants that are cultivated under circumstances wherein the high infectivity and persistence of CGMMV can be a major problem, such as the cultivation of cucumbers in greenhouses. When generating a resistance of an extreme nature it is preferred that not even low levels of accumulation of viral RNA in the resistant plants is tolerated.

[0052] In one aspect of the present invention, this problem is solved by transforming a plant with a polynucleotide sequence (e,g. as part of a genetic construct) that is capable of including resistance against CGMMV by a mechanism that triggers sequence-specific gene silencing.

[0053] Induction of PTGS (Post-transcriptional gene silencing) is a method to obtain down-regulation of gene expression of genes homologous to the inducing sequence. It has previously been employed to down regulate endogenous genes or transgenes. The present invention employs this principle for the silencing of viral genes and more in particular CGMMV genes. The natural mechanism of PTGS is not entirely understood. Plant viruses however, have evolved to overcome or suppress PTGS in order to be infective. The efficacy of PTGS against viruses has therefor not yet proven to be a wide-spread or general mechanism. The efficacy of PTGS and similar concepts will therefore largely if not mainly depend an the evolutionary development of the plant in question as well as the virus concerned. PTGS is considered to be sequence specific and it has been theorised that induction occurs by aberrant forms of RNA homologous to the genes. Aberrant form of RNA are for example extremely high levels. Of specific RNA molecules such as appear after viral infection of plant cells. Hence, it appears that sequence-specific gene silencing is induced by either high levels of transgene transcription or by the production of aberrant RNA.

[0054] One of a number of ways of inducing sequence-specific gene silencing is by expressing in a cell sense and antisense RNA molecules. These sense and antisense RNA molecules comprise nucleotide sequences respectively homologous and complementary to at least part of the nucleotide sequence of the nucleic acid of interest. In the case the nucleic acid of interest derives from a virus, the nucleotide sequence is (art of) a viral gene, for instance a gene encoding for a coat protein, a movement gene or a replicase gene.

[0055] The sense and antisense RNA molecules may be provided as one RNA molecule, for instance in the form of one or more inverted repeat sequences. Alternatively the sense and antisense RNA molecules may be provided as (a part) of two or more RNA moleculear. The sense and antisense RNA may be linked by a spacer nucleotide sequence.

[0056] Without be bound thereto, the theory is that the sense and antisense RNA are capable of forming a double stranded RNA molecule (dsRNA). The dsRNA subsequently triggers a sequence specific RNA degradation mechanism. This phenomenon has been observed in a variety of organisms such as C. elegans, Drosophila and Arabidopsis (see or example Chuang, Z, Marcowitz, Proc. Nat acad, Sci 2000, 97, 4985-4990). Alternatively the dsRNA causes hybrid arrest of translation of co-factors required for viral replication or the hybridization of the RNA affects intra-molecular base pairing required for viral replication. At present and for the purposes of the present invention there is no preference for either theoretical mechanism. The use of gene silencing in relation to inducing virus resistance has been described previously in a number of articles such as by Waterhouse et al. in Trends in Plant Science, 1999, 4, 452-457; Kooter et al. in Trends in Plant Science, 1999, 4, 340-347; Andrew Fire in Trends In Genetics 1999, 15, 358; Muskens et al. in Plant Molecular Biology 2000, 43, 243-260.

[0057] The present invention provides a method for generating resistance in a plant or in a plant cell or against infection with CGMMV, said method comprising at least each step of transforming said plant or plant cell with one or more polynucleotide sequence that upon (at least) transformation into a plant and transcription into RNA generates resistance against infection wit CGMMV in said plant, preferably upon (at least) transformation into a plant and transcription into RNA the polynucleotide sequence does not lead to generation of (any) replicase activity in said plant; wherein the one or more polynucleotide sequence(s) comprises a first and a second DNA sequence, wherein the first DNA sequence comprises a promoter operably linked to a first DNA region capable of being transcribed into a sense RNA molecule comprising a nucleotide sequence of at least 10 consecutive nucleotides having between 75 and 100% sequence identity with at least part of the nucleotide sequence of the genome of a CGMMV virus; and preferably a further DNA region capable of controlling transcription termination and/or polyadenylation in the plant or plant cells, whereby the further DNA region is operably linked to the first DNA region. The second DNA sequence comprises a promoter operably linked to a second DNA region capable of being transcribed into an antisense RNA molecule comprising an nucleotide sequence including at least 10 consecutive nucleotides, having between about 75% to about 100% sequence identity with the complement of at least 10 consecutive nucleotides of the sense nucleotide sequence; and preferably a further DNA region capable of controlling transcription termination and polyadenylation in the plant or plant cells, The sense and antisense RNA molecules are capable of forming a double stranded RNA region by base-pairing between the regions which are complementary. Preferably, transforming the plant with the nucleotide sequence according to the invention and transcription of the nucleotide sequence into RNA does not lead to generation of (any) replicase activity in said plant. The first and second DNA sequence are either integrated separately, for instance in different loci in the nuclear gene of the transformed cell or they are linked on one recombinant DNA (i.e. one locus) such that DNAs are integrated together in the nuclear genome of the transgenic plant cells.

[0058] In order to provide resistance in the present invention, the nucleotide sequence derived from the genome of a CGMMV virus may be from a strain of the virus that in itself is not capable of infecting the plant, but which sequence is suitable for the generation of resistance against tobamoviruses in general and CGMMV and in particular.

[0059] The polynucleotide sequence according to the invention or at least apart thereof is preferably capable of forming at least one double strained RNA molecule by complementary base pairing of at least part of the sense and antisense RNA sequences. The polynucleotide according to the present invention is in general capable of virus induced gene silencing or similar mechanisms as herein described, resulting in the generation of resistance, preferably extreme resistance of the plant cells against CGMMV.

[0060] Preferably, the first and second DNA regions, encoding the sense and antisense RNA molecule, are derived from the nucleotide sequence encoding the RNA dependent RNA polymerase of CGMMV. Other nucleotide sequences derived from CGMMV are also suitable for the generation the first and second DNA regions according to the invention, based on the presently provided nucleotide sequence of CGMMV. In a preferred embodiment, a fragment derived from a nucleotide sequence encoding a RNA dependent RNA polymerase, preferably from CGMMV, is cloned in inverted repeat orientation, separated by a stuffer fragment. Transcription of the fragment in this arrangement will produce an RNA molecule that is capable of framing a hairpin structure. These constructs are evaluated in cucumber as will be further explained in the examples below. The use of dsRNA in a method for inducing vis resistance has been previously described in WO 99/53050. In this particular case, tobacco was transformed to obtain transgenic tobacco resistant against Potato Virus Y (PVY). The experiments showed that transforming plants with specifically designed constructs that contain a PVY protease sequence in only a sense orientation or only an antisense orientation resulted in virus resistance in 4 to ca. 10% of Me total number of treated plants. Improved restistance was found when the construct contained said PVY protease sequence in both a sense orientation and an antisense orientations WO 99/53050 hence teaches that in tobacco plants that are already susceptible of being rendered resistant by either a selected sense or a selected antisense sequence of said PVY protease alone, restistance may be improved by modifying the constructs to such that they express both sense and antisense RNA sequences.

[0061] Little is known at present regarding the defense mechanism against viruses in the Cucurbitaceae fly. Cucumber, as an example of the Cucurbitaceae lily is known to be highly susceptible to a wide variety of viruses and has, due to this susceptibility in certain cases even been used as a diagnostic tool for the detection of viruses. It has bee n hypothesized that his may be due to the fact that the antiviral defense mechanisms in the Cucurbitaceae lily are not well developed. In the art, hence, no knowledge is available that provides guidance to the skilled man that the mechanism for conferring resistance described in the case of PVY infections in tobacco can easily be modified or transferred to other plants, especially to the Cucurbitaceae fly without undue experimentation and with a reasonable expectation of succes. This holds especially in the case of the Cucumber Green Mottle Mosaic Virus, of which the nucleotide sequence has only now been made available by the present applicants.

[0062] Furthermore, WO 99/53050 provides no insight or set of teachings that cat guide the skilled man in the process of selecting the parts of the sequence of CGMMV that when transformed into a plant cell are capable of conferring resistance to other viruses than Potato Virus Y in general, and to members of the Tobamovirus group of viruses in particular. Potato Virus Y is a member of the Polyvirus group, whereas CGMMV is a member of the Tobamovirus group. Although both viral groups are characterized by viral genomes consisting of one single positive RNA strand (positive mug that the single strand RNA encodes the viral proteins directly, as opposed to viral proteins being encoded by a complementary RNA molecule synthesized from the genomic RNA stand), they employ completely different replication strategies. Potyviruses encode on their RNA one single Open Reading Frame, that upon infection in plant cells is being translated into a single large polyprotein This polyprotein is subsequently cleaved and processed into the various functional viral proteins by protease activity provided by the polyprotein itself. WO 99/53050 teaches the use of sense and antisense nucleotide sequences derived from that part of the potyvirus gernome, that encodes the protease domains. Thus, sequence-specific degradation directed toward this particular part of the potyvirus genome will at least prevent the transition of peptides with this protease activity.

[0063] Tobamoviruses in general, and CGMMV in particular, do not encode proteases or protease activity. Instead, upon infection of a plant cell with these types of viruses, tile most 5′ located Open Reading Frame of the viral genome will be translated into a functional RNA dependent RNA polymerase (RdRP, also termed ‘replicase’), that, in turn is capable of not only replicating the entire viral genomic RNA, but that more specifically will generate subgenomic RNA molecules from the 3′ part of the viral genome. These subgenomic RNA molecules encode the more 3′ located viral Open Riding Frames, from which the movement proteins and coat proteins are the translated. In view of this totally different replication strategy in Tobamoviruses, the choice of the nucleotide sequences to be employed in sense and antisense gene constructs of the present invention cannot be deduced from WO 99/53050.

[0064] In a preferred embodiment of the present invention, the sense and antisense RNA molecules may be provided as one single RNA molecule, wherein preferably but not necessarily, the sense and antisense RNA sequence may be linked together through a spacer nucleotide sequence and are capable of forming a double stranded RNA molecule, also referred to as a hairpin structure. Providing the sense and antisense RNAs ma single molecule has the advantage that the ability to form a double stranded RNA molecule will become independent from the concentrations of the sense and a&sense RNAs.

[0065] The spacer nucleotide sequence is preferably located between the sense and antisense nucleotide sequence. The spacer sequence is preferred for stability of the gene constructs in the process of gene cloning. In the absence of such a spacer sequence, the RNA molecule will still be able to form a double-stranded RNA, particularly if the sense and antisense nucleotide sequence are larger than about 10 nucleotides and part of the sense and/or antisense nucleotide sequence will be used to form the loop allowing tie base-pairing between the regions with sense and antisense nucleotide sequence and formation of a double stranded RNA. There are no length limits or sequence requirements associated with the spacer region, as long as these parameters do not interfere with the capability of the RNA regions with the sense and antisense nucleotide sequence to form a double stranded RNA. Hence the spacer may comprise artificial sequences that preferably are designed to aid in formation of the loop. The spacer, in a preferred embodiment, comprises an intron. In a preferred embodiment, the spacer region varies in length from 4 to about 2000 bp, preferably from 50 to 1500 bp, more preferably from 100-1250 bp. However, as previously mentioned, may be absent in which case the sense and antisense RNAs will be directly linked to each other.

[0066] In the present invention of generating resistance, preferably extreme resistance against CGMMV, it is preferred that the genetic conduct that is used for triggering the RNA degradation mechanism is formed by a sequence that comprises a promoter, operably linked to a first DNA sequence in sense direction, optionally followed by a spacer, followed by a second DNA sequence in antisense direction, optionally followed by a DNA sequence capable of controlling transcription termination or polyadenylation.

[0067] The genetic construct of the invention encode RNA molecules capable of forming more than one secondary structures such as hairpins or stem-loop sutures. Preferably, the genetic constructs of the invention are designed that hey encode an RNA, molecule capable of adopting a secondary structure of the RNA has the lowest free energy, preferably under physiological conditions (as they may occur in the cell). In accordance with the invention, the RNA molecule to be produced in the cell is designed in such a way that at least in its lowest free energy state, which it can assume under physiological conditions (within the cell), it will comprise the desired hairpin.

[0068] As used herein “hairpin RNA” refers to any self-annealing double stranded RNA molecule. In its simplest representation, a hairpin RNA consists of a double studded stem made up by the annealing RNA stands, connected by a single RNA loop, and is also referred to as a “pan-handle RNA”. However, the term “hairpin RNA” is also intended to encompass more complicated secondary RNA structures comprising self-annealing double stranded RNA sequences, but also internal bulges and loops. The specific secondary structure adapted will be determined by the fee energy of the RNA molecule, and can be predicted for different situations using appropriate software such as FOLDRNA (Zuker and Stiegler, 1981).

[0069] As used herein, the term “plant-expressible promoter” or “promoter” means a DNA sequence which is capable of controlling (initiating) transcription in a plant cell. This includes any promoter of plant origin, but also any promoter of non-plant origin which is capable of directing transcription in a plant cell, i.e., certain promoters of viral or bacterial origin such as the CaMV35S, the subterranean clover virus promoter No 4 or No 7, or T-DNA gene promoters. It is preferred to use a promoter that has been reported active is cucumber for example, and preferred 35S.

[0070] The term “expression of a gene” refers to the process who a DNA region which is preferably linked to appropriate regulatory regions, particularly to a promoter, is transcribed into an RNA which is biologically active i.e., which is either capable of interaction with another nucleic acid or which is capable of being translated into a polypeptide or protein A gene is said to encode an RNA when the end product of the expression of the gene is biologically active RNA, such as e.g. an antisense RNA, a ribozyme or a replicative intermediate. A gene is said to encode a protein when the end product of the evasion of the gone is a protein or polypeptide.

[0071] As used herein, “reduction of expression of the target nucleic acid” refers to the comparison of the expression of the nucleic acid of interest in the eucaryotic cell in the presence of the RNA or chimeric genes of the invention, to the expression of the nucleic acid of interest in the absence of the RNA or chimeric, genes of the invention, The expansion in the presence of the chimeric RNA of the invention should thus be lower than the expression in absence thereof; preferably be only about 25%, particularly only about 10%, more particularly only about 5% of the expression of the target nucleic acid in absence of the clnmeric RNA, especially the expression should be completely inhibited for all practical purposes by the presence of the chimeric RNA or the chimeric gene encoding such an RNA. The present invention preferably provides for sequence specific RNA degradation mechanism that leads to the essential annihilation of the viral genome.

[0072] A nucleic acid of interest is “capable of being expressed”, when said nucleic acid, when introduced in a suitable host cell, particularly in a plant cell, can be transcribed (or replicated) to yield an RNA, and/or translated to yield a polypeptide or protein in that host cell.

[0073] As used herein “a nucleic acid of interest” or a “target nucleic acid” refers to any particular RNA molecule or DNA sequence which may be present in a eucaryotic cell, particularly a plant cell. The term “gene” means any DNA fragment comprising a DNA region (the “transcribed DNA region”) that is transcribed into a RNA molecule (e. g., an mRNA) in a cell operably linked to suitable regulatory regions, e. g., a plant-expressible promoter. A gene may thus comprise several operably linked DNA fragments such as a promoter, a 5′leader sequence, a coding region, and a 3′region comprising a polyadenylation site. A plant gene endogenous to a particular plant species (endogenous plant gene) is a gene which is naturally found in that plant species or which can be introduced in that plant species by conventional breeding. A chimeric gene is any gene which is not normally found in a plant species or, alternatively, any gene in which the promoter is not associated in nature with part or all of the transcribed DNA region or with at least one other regulatory region of the gene.

[0074] As used herein, “sequence identity” with regard to nucleotide sequences (DNA or RNA), refers to the number of positions with identical nucleotides divided by the number of nucleotides in the shorter of the two sequences. The alignment of the two nucleotide sequences is performed by the Wilbur and Lipmann algorithm (Wilbur and Lipmann, 1983) using a window-size of 20 nucleotides, a word length of 4 nucleotides, and a gap penalty of 4. Computer-assisted analysis and interpretation of sequence data including sequence alignment as described above, can, a. g., be convenietly performed using the programs of the Intellligentics Suite (Intelligenetics Inc., CA). Sequences are indicated as “essentially similar “when such sequence have a sequence identity of at leas about 75%, particulmly at least about 80%, more particularly at leastabout 85%, quite particularly about 90%, especially about 95%, more especially about 100%, quite especially are identical. It is clear than when RNA sequences are said to be essentially similar or have a certain degree of sequence identity with DNA sequences, thymine (T) in the DNA sequence is considered equal to uracil (U) in the RNA sequence.

[0075] It is an object of the invention to provide a virus resistant plant, comprising a first and second chimeric DNA integrated in the nuclear genome of at least some of its cells, wherein the first chimeric DNA comprises a plant-expressible promoter, operably liked to a first DNA region capable of being transcribed into a sense RNA molecule comprising a nucleotide sequence of at least 10 consecutive nucleotides having between 75 and 100% sequence identity with at least part of the nucleotide sequence of the genome of a virus capable of infecting the plant, and optionally a DNA region involved in transcription termination and polyadenylation functioning in plant cells. The second chimeric DNA comprises a plant-expressible promoter, operably linked to a second DNA region capable of being transcribed into an antisense RNA molecule comprising an antisense nucleotide sequence including at least 10 consecutive nucleotides, having between about 75% to about 100% sequence identity with the complement of the at least 10 consecutive nucleotides of the sense nucleotide sequence, and optionally a DNA region involved in transcription termination and polyadenylation functioning in plant cells. Preferably the at least 10 nucleotides share sequence identity with part of the vial genome that encodes a replicase function, and more preferably the virus is a CGMMV.

[0076] The sense and antisense RNA molecules are capable of forming a double stranded RNA region by base-pairing between the regions which are complementary. The first and second chimeric DNA are integrated either in one locus or in different loci in the nuclear genome.

[0077] In a preferred embodiment of the invention, the RNA molecule transcribed from the chimeric gene, consists essentially of the hairpin RNA.

[0078] In a preferred embodiment, the order of the sense and antisense nucleotide sequence in the RNA molecule is not critical.

[0079] Thus, in other words, the chimeric DNA ha a transcribed DNA region, which when transcribed, yields a RNA molecule comprising an RNA region cable of forming an stem-loop structure, wherein one of the annealing RNA sequences of the stem-loop Lecture comprises a sequence, essentially similar to at least part of the nucleotide sequence of the nucleic acid of interest, and wherein the second of the annealing RNA sequences comprises a sequence essentially similar to at least part of the complement of at least part of be nucleotide sequence of the nucleic acid of interest The RNA molecule may comprise more than one hairpin structures, which may be designed to reduce the expression of diffent nucleic acids of interest.

[0080] In a preferred embodiment, the nucleic acid of interest, whose expression is targeted to be reduced or whose degradation is desired, is a viral nucleic acid, particularly a viral RNA molecule, more in particular a tobamovirus, most in particular a CGMMV RNA molecule capable of infecting a eucaryotic cell, particularly a plant cell In a preferred embodiment, the expression to be reduced is the replication of the virus and/or the degradation of the viral DNA It is also preferred to reduce or to remove the disease symptoms caused by the infecting virus. The reduction of expression or the degradation of other genes from CGMMV such as the genes encoding for movement proteins or coat proteins or the degradation of other viral nucleic acid sequences or the degradation of subgenomic RNAs is also explicitly included within the scope of the present invention

[0081] Preferably, the nucleotide sequence of the target nucleic acid corresponding to the sense nucleotide sequence is part of a DNA region which is transcribed, particularly a DNA region which is transcribed and translated (in other words a coding region). It is particularly preferred that the target sequence corresponds to one or more consecutive exons, more particularly is located within a single exon of a coding region.

[0082] The length of the sense nucleotide sequence may vary from about 10 nucleotides (nt) up to a length equaling the length (in nucleotides) of the target nucleic acid Preferably the total length of the sense nucleotide sequence is at least 10 nt, preferably 15 nt, particularly at least about 50 nt, more particularly at least about 100 nt, especially at least about 150 nt, more especially at least about 200 nt, quite especially at least about 550 nt. In principle there is no upper limit for the total length of the sense nucleotide sequence, other than the total length of the target nucleic acid However for purely practical reason (such as e. g. stability of the chimeric genes, ease of manipulating the genetic constructs) the length of the sense nucleotide sequence should preferably not exceed 5000 nt, more preferably should not exceed 2500 nt and may preferably be limited to about 1000 nt.

[0083] It will be appreciated that the longer the total length of the sense nucleotide sequence is, the less stringent the requirements for sequence identity between the total sense nucleotide sequence and the corresponding sequence in the target gene become. Preferably, the total sense nucleotide sequence should have a sequence identity of at least about 75% with the corresponding target sequence, particularly at least about 80%, more particllarly atleast about 85%, quite particularly about 90%, especially about 95%, more especially about 100%, quite especially be identical to the corresponding part of the target nucleic acid. However, it is preferred that the sense nucleotide sequence always inrludes a sequence of about 10 consecutive nucleotides, partcularly about 20 nt, more particularly about 50 nt, especially about 100 nt, quite especially about 150 nt with 100% sequence identity to the coresponding part of the target nucleic acid. Preferably, for calculating the sequence identity and designing the corresponding sense sequence, the number of gaps should be minimized, particularly for the shorter sense sequences.

[0084] The length of the antisense nucleotide sequence is largely den ed by the lens of the sense nucleotide sequence, and will preferably correspond to the length of the latter sequence. However, it is possible to use an antisense sequence which differs in length by about 10%. Similarly, the nucleotide sequece of the antisense region is largely det rniued by the nucleotide sequence of the sense region, and preferably is identical to the complement of the nucleotide sequence of the sense region. Particularly with longer antisense regions, it is however possible to use antisense sequences with lower sequence identity to the complement of the sense nucleotide sequence, preferably with at least about 75% sequence identity, more preferably with at least about 80%, paticully with at ls about 85%, more partcularly with at least about 90% sequence identity, especially with at least about 95% sequence to the complement of the sense nucleotide sequence. Nevetheless, it is preferred thbat the antisense nucleotide sequences always includes a sequeace of about 10, preferably 15 consecutive nucleotides, particularly about 20 nt more particularly about 50 nt, especially about 100 nt, quite especially about 150 nt with at least 80%, preferably at leas 90% more preferably at least 95% and most preferred 100% sequence identity to the complement of a correponding part of the sense nucleotide sequence. Again preferably the number of gaps should be minimized, particuarly for th shorter antisense sequences. Further, it is also preferred that the antisense sequence has between about 75% to 100% sequence identity with the complement of the target sequence.

[0085] In a preferred embodiment the hairpin RNA formed by the sense and antisense region and if appropriate the spacer region, is an hairpin RNA.

[0086] By “artificial hairpin RNA” or “artificial stem-loop RNA structure”, is meant that such hairpin RNA is not naturally occuring in nature, because the sense and antisense regions as defined are not naturally occurring simultaneously in one RNA molecule, or the sense and antisense regions are separated by a spacer region which is heterologous with respect to the target gene, particularly, the nucleotide sequence of the spacer has a sequence identity of less than 75% with the nucleotide sequence of the target sequence, at the corresponding location 5′ or 3′ of the endpoints of the sense nucleotide sequence. A hairpin RNA can also be indicated as artificial, if it is not coded within the RNA molecule it is nay associated with It is conceivable to use in accordance with the invention a chimeric DNA whose transcription results in a hairpin RNA structure with a naturally occurring nucleotide sequence (which otherwise meets he limits as set for i this specification) provided this hairpin RNA is devoid of the subsiding RNA sequences (not involved in the hairpin structure formation).

[0087] Although it is preferred that the RNA molecule comprising the hairpin RNA does not further comprise an intron sequence, it is clear that the chimeric DNA genes encoding such RNAs may comprise in their transcribed region one or more introns.

[0088] The transformed plant cells are preferably used for the generation of transformed plants that can be fisher used in conventional breeding schemes to provide for more plants or to introduce the desired transformation, in the present invention resistance against CGMMV, to other varieties of the same or related plant species or in hybrid plants. Seeds obtained from the transformed plants containing the chimeric genes of the invention are also encompassed within the presently claimed scope.

[0089] As herein defined, with “inverted repeat sequence” is meant a DNA or RNA sequence that contains two identical nucleotide sequences in opposite directions (i.e. sense and anti-sense). The identical nucleotide sequences may be divided by a spacer. Identical in this respect is to be seen in the terms of sequence identity as herein defined.

[0090] The RNA sequence of the viral genome that may be used in the design of a suitable construct for use in the present invention preferably comprises nucleotides sequences that are derived from nucleotides sequences of the virus of interest in the present case and preferably CGMMV, encoding (part(s) of) the movement, coat and/or replicase proteins, of which nucleotide sequences coding for the replicase protein are most preferred However, other nucleotide sequences that can be expressed such that resistance is conferred by virus-derived transgenes are included within the present invention, Such nucleotide sequences are sequences that are homologous, preferably functionally homologous, to the sequences of the present invention. The term homologous in terns of the present invention indicates a certain amount of sequence identity on the nucleotide level. 100% homology indicates that the sequences are 100% identical. Sequences are also considered homologous if one or more nucleotides from the sequence are deleted, added or replaced as long as a certain percentage of sequence identity remains, for instance with a most preferred limit of 99%, more preferably 95, 85, 80, preferably 75, 70 or 65%. Also percentages as low as 50 or 60% may very well be considered as homologous. Whether or not a squence can be regarded as homologous also depend on the function of that sequence. For instance a nucleotide sequence encoding for a protein will still be considered as homologous if the protein it encodes for is able to perform its function. Hence homology is present if the functionality is maintained, thereby allowing for well known principles as degeneracy. By the term “functionally homologous” is meant the following. A sequence (for instance a gene) is considered functionally homologous if that sequence (gene) is homologous to another sequence, hence at least one nucleotide is deleted, inserted, replaced such as inversed (in case of more than one nucleotide) or transversion or transition while the function of said sequence (gene) is substantially maintained. This may also apply to chemically modified sequences. When a sequence is functionally homologous, there may very well be a low percentage of homology, but the functionality of that sequence is substantially maintained. Such sequences, whether DNA or RNA are also included within the scope of the present invention.

[0091] In a preferred embodiment, the sequence used to design the construct of the present invention is the “nucleotide sequence encoding a defective variant of the replicase gene of CGMMV” as herein defined.

[0092] In another aspect of the present invention, this problem is solved by transforming a plant with a polynucleotide sequence (e.g. as part of a genetic construct) that can provide the plant with so-called “replicase-mediated” resistance against CGMMV. In particular, this will be a polynucleotide sequence that

[0093] i) has been derived from the 129 kD sequence, the 57 kD sequence, or the 186 kD readthrough sequence of native CGMMV;

[0094] ii) upon (at least) transformation into the plant and transcription into RNA—and usually also translation into the corresponding encoded protein—can provide the plant with resistance against CGMMV; but

[0095] iii) does not encode any replicase activity.

[0096] In one aspect of the invention, in case of the “replicase-mediated” resistance, a polynucleotide sequence according to the invention can encode a polypeptide or protein that is capable of providing a plant with resistance against GCMMV, but that by itself has no replicase activity, for resistance due to one or more alterations in its amino acid sequence, compared to the o acid sequence encoded by the 129 kD sequence, 57 kD sequence, and/or 186 kD readthrough sequence of native CGMMV.

[0097] However, according to one specific embodiment of the invention, the polynucleotide sequence may also comprise, or even consist of the native 57 kD sequence.

[0098] In one aspect, the invention therefore relates to a method for genetic resistance in a plant against CGMMV, said method comprising at least the step of transforming said plant with a polynucleotide encoding a defective variant of the replicase gene of CGMMV.

[0099] In another aspect, the invention also relates to a method for providing a transgenic plant and/or plant cell that is resistant against infection with CGMMV, comprising at least the step of transforming said plant or plant cell with a polynucleotide sequence encoding a defective variant of the replicase gene of CGMMV.

[0100] In another aspect, the invention also relates to a genetic construct suitable for transforming a plant, said construct at lost comprising a polynucleotide sequence encoding a defective variant of the replicase gene of CGMMV, and optionally further elements of genetic constructs known per se. The invention also relates to a plant, plant cell and/or plant material that has been transformed with a genetic construct of the invention.

[0101] The invention also relates to transgenic, p s that contain a polynucleotide sequence encoding a defective variant of the replicase gene of CGMMV, and/or that have been provided with resistance against infection with CGMMV by the method of the invention.

[0102] In the context of the invention, by the “replicase gene of CGMMV” is meant the native 129 kD sequence, the native 57 kD sequence, and/or the combined native 186 kD “readthrough” product of the native 129 kD and native 57 kD sequences.

[0103] By a “native” sequence is any RNA sequence that naturally occurs in CGMMV, including all isolates and strains thereof, as well as any DNA sequence that corresponds to these naturally occurring RNA sequences. Examples of such native sequences are the 129 kD nucleotide sequences given in SEQ. ID no.1 and SEQ. ID no.17, the 57 kD nucleotide sequences given in SEQ. ID no.3 and SEQ. ID no.19 and the 186 kD nucleotide sequences given in SEQ. ID no.5 and SEQ. ID no.21. It will be clear to the skilled person that there may be (further) naturally occurring variants of the RNA sequence from which the DNA sequences in the sequence listings were derived, and these (and the DNA sequences corresponding thereto) are also included within the term “native sequence”.

[0104] By “a polynucleotide sequence encoding a defective variant of the replicase gene of CGMMV” in its broadest sense is meant a polynucleotide sequence that

[0105] i) upon (at least) transformation into a plant and transcription into RNA generates resistance against infection with CGMMV in said plant; and

[0106] ii) upon (at least) formation into a plant and transcription into RNA does not lead to generation of (any) replicase activity in said plant (or at least when it does lead to expression of some replicase activity—leads to expression of a replicase activity that is severely reduced compared to expression of the native gene encoding CGMMV replicase).

[0107] Herein, the terms “plant”, “transformed plant” and/or “transgenic plant” include all parts or tissues of such a plant including but not limited to individual cells of such a plant. These terms also includes material of or for such a plant, such as material that can be regenerated into a (ire) plant, including but not limited to protoplasts and/or callus tissue, or material that can be cultivated into a mature plant, such as cultivation material.

[0108] The plant is preferably a pit that is susceptible to infection with CGMMV, more preferably a plant belonging to the Cucurbiteceae family, such as melon (Cucumis melo), cucumber (C. sativus), watermelon (Citrullus vulgaris) and bottlegourd (Lagenaria siceraria).

[0109] Included within the term “CGMMV” are all known strains thereof, including those prevalent in Europe and Asia. In particular, the method of the invention can be used to protect plants against strain of GCMMV prevalent in Europe (including Israel), such as those which are a problem in the cultivation of melons and in particular cucumbers in greenhouses, although the invention is not limited thereto.

[0110] In doing so, a major advantage of the invention is that it can provide protection against several and preferably all, (such) strains of CGMMV simultaneously. Another advantage of the invention is that it provides “absolute” protection against CGMMV, which means that—upon expression of a polynucleotide sequence encoding a defective replicase in a plant—essentially no viral particles can be detected in the transformed plant (material). The method of the invention therefore does not lead to a deferral or slowing down of the onset of symptoms, as may occur when so-called “coat protein-mediated” resistance is used. Also, the method of the invention leads to a high level of resistance, and may also have the advantage of a favorable temperature effect. Usually, the “nucleotide sequence encoding a defective variant of the replicase gene of CGMVV” will be a nucleotide sequence in which—compared to a nucleotide sequence encoding the corresponding native replicase of CGMMV—one or more nucleotides have been added, replaced and/or removed. In particular, the “nucleotide sequence encoding a defective variant of the replicase gene of CGMMV may be a nucleotide sequence that comprises, and preferably consists of:

[0111] a nucleotide sequence corresponding to the native 129 kD sequence in which—compared to said native sequence—one or more nucleotides have been added, replaced and/or removed;

[0112] a nucleotide sequence corresponding to the native 186 kD sequence in which—compared to said native sequence—one or more nucleotides have been added, replaced and/or removed, e.g. in the part of the native 186 kD sequence corresponding to the 129 kD sequence, to the 57 kD sequence, or both;

[0113] a nucleotide sequence corresponding to the native 57 kD sequence;

[0114] a nucleotide sequence corresponding to the native 57 kD sequence in which—compared to said native nucleotide—one or more nucleotides have been added, replaced and/or removed;

[0115] such that said nucleotide sequence is capable—upon (at least) transformation into a plant and transcription into RNA—to confer to said plant resistance against iron with CGMMV, and such that said nucleotide sequence—upon (at least) transformation into a plant and transcription into RNA—is not capable of generating of(any) replicase activity in said plant.

[0116] Usually, the “nucleotide sequence encoding the defective variant of the replicase gene of CGMWV will encode a protein or polypeptide, more specifically a protein or polypeptide that:

[0117] 1) upon being expressed in a plant is capable of generating resistance against CGMMV in said plant; and

[0118] 2) upon being expressed in a plant has no replicase activity (or when it has some replicase activity—has severely reduced replicase activity compared to the native CGMMV replicase).

[0119] Such a protein or polypeptide will be generally referred to hereinbelow as “defective replicase”; and a polynucleotide sequence encoding such a protein or polypeptide will be referred to as a “polynucleotide sequence encoding a defective replicase”.

[0120] Usually, the defective replicase will be a derivative—such as an analog, homolog, variant, mutant, part fragment or combination of two or more such parts or fragments, etc.—of the amino acid sequence encoded by the native 129 kD sequence, the native 186 kD sequence and/or the native 57 kD sequence, in which—compared to the amino acid sequence encoded by the corresponding native sequence—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed, leading to loss of replicase activity (or at least an inability to generate replicase activity wheb expressed in the plant).

[0121] In particular, the defective replicase may be a protein or polypeptide that comprises, and preferably consists of:

[0122] an amino acid sequence corresponding to the amino acid sequence encoded by the native 129 kD sequence in which—compared to said native sequence—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed;

[0123] an amino acid sequence corresponding to the amino acid sequence encoded by the native 186 D sequence, in which—compared to said native sequence—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed, leading to loss of replicase activity;

[0124] an amino acid sequence corresponding to the ammo acid sequence encoded by native 57 kD sequence;

[0125] an amino acid sequence corresponding to the amino acid sequence encoded by the native 57 kD sequence, in which—compared to said native sequence—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed;

[0126] or any combination thereof, provided that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to generate resistance against CGMMV in said plant.

[0127] More in particular, the defective replicase may be a protein or polypeptide that comprises, and preferably consists of:

[0128] an amino acid sequence corresponding to a part or fragment of the amino acid sequence encoded by the native 129 kD sequence, or to a combination of two or more such parts or fragments;

[0129] an amino acid sequence corresponding to a part or fragment of the amino acid sequence encoded by the native 186 kD sequence, or to a combination of two or more such parts or fragments; or

[0130] an amino acid sequence corresponding to the amino acid sequence encoded by the native 57 kD sequence.

[0131] such that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to generate resistance against CGMMV in said plant.

[0132] An amino acid sequence “corresponding to apart or fragment of the amino acid sequence encoded by the native 186 kD sequence, or to a combination of two or more such parts or fragments” may for ice comprise: i) at least one part or fragment of the amino acid sequence encoded by the native 129 kD sequence combined with at least one part or fragment of the amino acid sequence encoded by the native 57 kD sequence (which combination of parts or fragments may or may not correspond to a contiguous amino acid sequence encoded by the native 186 kD sequence); ii) at least one part or fragment of the amino acid sequence encoded by the native 129 kD sequence combined with the full amino acid sequence encoded by the native 57 kD sequence, and/or iii) at least one part or fragment of the amino acid sequence encoded by the fill native 129 kD sequence combined with at least one part or fragment of the amino acid sequence encoded by he native 57 kD sequences.

[0133] It is know however, that expression in a plant of a nucleotide sequence encoding the full 129 kD sequence of the native replicase usually does not provide resistance against infection with CGMMV, but may even—upon infection of the plant—promote or facilitate multiplication of the virus. Therefore, in one embodiment the invention does not comprise the expression in a plant of said replicase, nor the use of a polynucleotide sequence encoding such a replicase.

[0134] Even more preferably, the defective replicase is a protein or polypeptide that consists of;

[0135] amino acid sequence corresponding to a part or fragment of the amino acid sequence encoded by the native 129 kD sequence, or a combination of two or more such parts or fragments; such that the resulting protein or polypeptide shows no replicase activity, but is still capable, upon expression in a plant to genome resistance against CGMMV in said plant, or

[0136] an amino acid sequence corresponding to the amino acid sequence encoded by the native 57 kD sequence.

[0137] Any such parts or fragments may also contain one or more further amino acid substitutions, insertions or deletions compared to the native sequence, but this is not preferred.

[0138] Most preferably, the defective replicase is a so-called “truncated replicase”, i.e. an amino add sequence corresponding to the amino acid sequence encoded either by the 129 kD sequence and/or by the 186 kD sequence, from which—compared to the native amino acid sequence—one or more amino acid residues are lacing at the carboxyl-terminus, such that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to genome resistance against CGMMV in said plant. (In case of a truncated replicase based upon the 186 kD sequence, this usually means that the resulting protein will contain the fill acid sequence of the 129 kD sequence, as well as part of the amino acid sequence of the 57 kD sequence (i.e. that is contiguous to the 129 kd sequence in the amino acid sequence encoded by native 186 kD sequence), with one or more amino acids lacking at the carboxy-terminus of the 57 kD part, although the invention its broadest sense is not limited thereto).

[0139] The polynucleotide sequence that encode such a tuncated replicase may either comprise, or preferably consist of the full native 129 kD sequence or 186 kD sequence, respectively, in which a stopcodon has been introduced at a desired site, or a polynucleotide sequence from which—compared to the full native 129 kD sequence or 186 kD sequence, respectively—one or more codons coding for the carboxy-terminal amino acid residues have been removed, i.e. starting from the 3 ′end of the native sequence(s).

[0140] As mentioned below, preferably a stopcodon is introduced in to the native sequence, in particular in the so-called GDD motiv or in the P-loop. Examples thereof are the polynucleotide sequences comprised in the vectors shown in FIGS. 3-8, and as described in the Experimental Part.

[0141] Again, any such truncated replicase may also contain one or more amino acid substitutions, insertions or deletions compared to the native sequence, but this is not preferred.

[0142] As mentioned above, (the polynucleotide sequence encoding) the defective replicase is such that—after expression in a plant or plant cell—it is still capable of generating resistance against CGMMV in said plant. Usually, this means that the defective replicase will have at least one biological function that allows the defective replicase to protect the plant against CGMMV infection, such as for example down-region of viral replication or interference with the replication of the wild-type CGMMV, for instance by competing with wild-type virus for the replication machinery in the plant (cell). It will be clear that in order to achieve such a biological function, the defective replicase must usually have a certain minimal level of amino acid similarity wit the amino acid sequences encoded by the native 129 kD, 186 kD and/or 57 kD sequences. In so far as the defective replicase is s to the corresponding native amino acid sequence, this may be because it contains—on the corresponding amino acid positions—the same amino acid residues as the native amino acid sequence, or amino acid residues comparable thereto. The latter will usually comprise so-called “conservative” amino acid substitutions, for instance involving replacing a given acidic or basic amino acid residue by another acidic or basic amino acid residue.

[0143] However, there will also be dies in amino acid sequence between the defective replicase and the native replicase (i.e. the 129 kD, 186 kD or 57 kD protein), such it the defective replicase will no longer provide replicase activity. The skilled person will be able to select appropriate alterations to the amino acid sequence of the native replicase. As will be clear to the skilled person, a single (amino acid or nucleotide) alteration may be sufficient, or two or more such alterations may be required, dependant upon the position and nature of the alteration(s) compared to the ammo acid sequence of the native replicase.

[0144] Whether a given polynucleotide sequence encodes a defective replicase according to the invention—or at least is capable of protecting a plant against infection with CGMMV—can simply be tested by transforming a plant, plant cell or plant material with a construct containing said polynucleotide sequence, and then exposing the plant, plant cell, plant material, and/or a mature plant generated therefore, to CGMMV under conditions such that infection may occur, It can then be easily determined whether the polynucleotide sequence/construct is capable of protecting the plant, i.e. by suitably determining the presence of the virus, or simply by the presence or absence of symptoms of CGMMV-infection.

[0145] In general, as a minimum, when the defective replicase contains my amino acid substitutions or insertions, it will have amino acid homology (i.e. identity on corresponding position) with the corresponding native replicase protein of at least 80%, preferably at least 90%, more preferably at least 95%, with amino acid deletions not being taken into account, and a single amino acid insertion being counted as a single alteration.

[0146] In general, as a minimum, when the defective replicase contains one or more amino acid deletions, it will usually contain at least 30%, preferably at least 50%, more preferably at least 70%, and usually 80-90%, and may even contain as much as 95-99%, of the amino cid sequence of the corresponding native replicase protin with any amino acid insertions or substtutions not being taken into account.

[0147] A truncated replicase based upon the 129 kD sequence will usually contain at least 50%, preferably at least 70%, and may contain as much as 80-95%, of the amino acid sequence of the native replicase. A truncated replicase based upon the 186 kD sequence may contain the full 129 kD protein followed by one or more amino acids from the 57 kD sequence, and usually contains the full 129 kD sequence followed by 1-95%, preferably 5-50%, of the 57 kD sequence.

[0148] The differences in acid sequence mentioned above can be differences compared to any of tie amino acid sequences given in SEQ ID's 2, 4, 6 and/or 18, 20, 22, and/or compared to any naturally occurring variant of these amino acid sequences. These differences are at least su that the resulting protein does not correspond to a naturally occurring/native protein (including those given in SEQ ID's 2, 4, 6 and/or 18, 20, 22).

[0149] The polynucleotide sequences used in the invention am such that they encode the above defective replicases. For this purpose, they may contain the same codons as in the corresponding positions on the native 129 kD, 186 kD and/or 57 kD sequence, or codons equivalent thereto due to the degeneracy of the genetic code.

[0150] The polynucleotide sequence encoding the defective replicase can be provided in a manner known per se, for instance starting from the known sequence of the native 129 kD, 57 kD and/or 186 kD sequences, and/or from a nucleic acid that encodes said sequences. Usually, this will involve introducing one or more deletions, substitutions and/or insertions of one or more nucleotides, or even of one or more codons into, or compared to, the native sequence. Such deletions, substitutions and/or insertions will be collectively referred to hereinbelow as “alterations”.

[0151] Accordingly, the polynucleotide sequence encoding the defective replicase may be a sequence that contain one or more such alterations compared to any of the nucleotide sequences given in SEQ ID's 1, 3, 5 and/or 17, 19, 21, and/or compared to any naturally occurring variant of these nucleotide sequences (including DNA sequences corresponding to the RNA sequences as present in the virus). These differences are at least such that the protein encoded by the polynucleotide sequence does not correspond to a naturally occurring native protein (including those given in SEQ ID's 2, 4, 6 and/or 16, 18, 22).

[0152] Furthermore, besides the alterations mentioned above, and compared to nucleotide sequences given in SEQ ID's 1, 3, 5 and/or 17, 19, 21 and/or compared to any naturally occurring variant of these nucleic acid sequences (including DNA sequences corresponding to the RNA sequences as present in the virus), the polynucleotide sequences may ether contain one or more alterations that lead to a codon that encodes the same amino acid as the codon given for the corresponding position in SEQ ID's 1, 3, 5 and/or 17, 19, 21, and this may even lead to a fully or totally artificial and/or synthetic sequence. Also, compared to nucleotide sequences given in SEQ ID's 1, 3, 5 and/or 17, 19, 21 and/or compared to any naturally occurring variant of these nucleic acid sequences (include DNA sequences corresponding to the RNA sequences as present ill the virus), the polynucleotide sequences may further contain one or more alterations that lead to a conservative amino acid substitution, i.e. as mentioned above.

[0153] Providing a polynucleotide sequence that contain the desired alterations will be within the skill of the artisan and can involve techniques such as nucleic acid synthesis using an automated nucleic acid synthesis technique; introduction of (point)mutations into a nucleic acid that comprises the native 129 kD, 57 kD, and/or 186 kD sequences; and/or using or suitably combining parts or gents of the 129 kD, 57 kD and/or 186 kD sequences, or any combination thereof. Also, in providing such a polynucleotide sequence, the skilled person may take into account the degeneracy of the genetic code and/or conservative amino acid substitutions, as mentioned above.

[0154] In order to provide a polynucleotide sequence that encodes a truncated replicase as defined above, a technique involving the introduction of a stopcodon into the native sequence is particularly preferred.

[0155] A particularly preferred technique of introducing the above alterations—including stopcodons—involves the use of a PCR reaction, in which the desired alterations are introduced into the amplified sequence(s) by the use of modified primers, i.e. primers that contain a suitable “mismatch” compared to the template sequence, leading to the desired alteration in the amplified sequence. This PCR-based technique may also be used to introduce one or more restriction sites into the amplified sequence in order to facilitate the cloning of the amplification products into the desired transfromation on vectors.

[0156] As further described in the Experimental Part, this may involve a single PCR-reaction, but may also involve two or more PCP, reactions, each leading to a pat of intended final sequence encoding the defective replicase in which the priers (e.g. with the desired alteration) form the ends of the fragments. These fragments may then be combined, for instance to provide a polynucleotide sequence that comprises a combination of such fragments, and/or to reconstitute the full 129 kD, 57 kD and/or 186 kD sequence, now containing the desired alteration compared to the native sequence, such as a stopcodon.

[0157] The PCR-reactions and the further steps following amplification, such as combining/joining the amplified sequences, can be carried out in a manner known per se, for instance as described in the Experimental Part and/or using the techniques described in U.S. Pat. No. 4,683,202; Saiki et al., Science 239 (1988), 487-491 or PCR Protocols, 1990, Academic Press, San Diego, Calif., USA.

[0158] As the template for the PCR-reaction a nucleic sequence encoding the native 129 kD, 57 kD and/or 186 kD sequence can be used, such as a cDNA derived from the native RNA sequence, or a paid containing such a sequence, including those described in the Experimental Part. The template used may itself already contain one or more alterations, compared to the corresponding native sequence.

[0159] As mentioned above, a preferred alteration involves the introduction of a stopcodon into the native 129 kD or 186 kD sequence, such that—upon transformation into a plant—the polynucleotide sequence thus obtained causes expression of a truncated replicase. In particular, such a stopcodon may be introduced into a sequence corresponding to the native 129 kD sequence, more in particular to that part of the native sequence that corresponds to the so-called GDD-motiv or to the so-called P-loop.

[0160] The polynucleotide sequence encoding the defective replicase is preferably in the form of—e.g. forms part of and/or is incorporated within—a genetic construct. The genetic construct is preferably a construct suitable for the transformation of a plant, plant cell and/or plant material, such as a plasmid, cosmid or vector, including co-integration vectors or by vectors. The genetic construct may be DNA or RNA, and is preferably dsDNA.

[0161] Preferably the genetic construct comprising the polynucleotide sequence encoding for the defective replicase is combed with the genetic construct comprising he polynucleotide sequence encoding for the hairpin sequence. By providing plants with these omnipotent constructs resistance can be generated against different suds of a virus, preferably the CGMMV virus, depending on the vulnerability of a strain for a particular method of generating resistance.

[0162] Such a construct may further contain all known elements for genetic constructs, and in particular for genetic constructs intended for the transformation of plants, as long as the presence thereof does rot interfere with the CGMMV resistance to be provided by the polynucleotide sequence encoding the defective replicase. Some non-limiting examples of such elements include leader sequences, terminators, enhancers, integration factors, selection markers, reporter genes, etc., and suitable elements will be clear to the skilled person.

[0163] These further elements may or may not be derived from plants, and may or may not be homologous to the plant that is to be transformed with the conduct of the invention (hereinbelow referred to as the “target plant”). For instance, the after elements may also have been derived from micro-organisms, viruses, etc., and may also be elements that are natively associated with the CGMMV sequence, such as the native CGMMV leader sequence (5′-UTR sequence).

[0164] The nucleotide sequences encoding these further elements may have been isolated and/or derived from a naturally occurring source—for instance as cDNA—and/or from known available sources (such as available plasmids, etc.), and/or may have been provided synthetically using known DNA synthesis techniques.

[0165] For instance, a construct of the invention will usually contain a suitable promoter operatively linked to the polynucleotide sequence encoding the defective replicase or the hairpin, e.g. such that it is capable of directing the expression of the polynucleotide sequence. Suitable promoters can be chosen from all known constitutive, inducible, tissue specific or other promoters that can direct expression of a desired nucleotide sequence in a plant and/or in part of a plant, including specific tissues and/or individual cells of the plant. In particular, promoters are used that are suitable for use in species of the Cucurbitaceae family, such as cucumber.

[0166] A specifically preferred promoter is the plastocyanine-promoter. Use of the 35S promoter is less preferred, as it may be less reliable in cucumber.

[0167] The terminator can be any terminator that is effective in plants. A particularly premed terminator is the nos-3′ terminator.

[0168] The selection marker can be any gene that can be used to select—under suitable conditions such as the use of a suitable selection medium-plants, plant material and plant cells that contain—e.g., as the result of a successful transformation—the genetic construct containing the marker, A particularly premed selection marker is the nptII-gene, which can be selected for using kanamycin.

[0169] The construct of the invention further preferably contains a leader sequence. Any suitable leader sequence, including those of viral origin, can be used. Preferably, a leader sequence essentially identical to the 5′untranslated (5′-UTR) region of the CGMMV genome is used. This may be derived from the viral RNA, or may be provided synthetically, e.g. as described in the Experimental Part.

[0170] Although not preferred, the invention also encompasses constructs that encode a fusion of a defective replicase as mentioned above, and at least one further amino acid sequence, such as a protein or polypeptide, or a part or fragment thereof, Preferably, expression of a defective replicase as (part of) such a fusion does not detract from the desired biological activity (i.e. protection against infection with CGMMV).

[0171] The construct of the invention can be provided in a manner known per se, which generally involves techniques such as restricting and linking nucleic acids/nucleic acid sequences, for which reference is made to the standard handbooks, such as Sambrook et al, “Molecular Cloning: A Laboratory Manual” (2nd ed.), Vols. 1-3, Cold Spring Harbor Laboratory (1989) of F. Ausubel et al, eds., “Current protocols in molecular biology”, Green Publishing and Wiley Interscience, New York (1987).

[0172] According to one embodiment, the genetic construct is preferably (also) in a form that can be maintained stable or inherited in a micro-organism, in particular a bacterium, more in particular a bacterium that can be used to transform a plant or plant material, such as Agrobacterium. In a further aspect, the invention also relates to such a micro-organism, in particular a bacterium, more in particular a bacterium tat can be used to transform a plant such as Agrobacterium, that contains a genetic construct according to the invention.

[0173] The genetic cons can be transformed into the target plant, plant cell or plant material by any suitable transformation technique known per se, including transformation with Agrobacterium, transformation with “denuded” DNA, for instance through particle bombardment or transformation of protoplast through electroporation or treatment with PEG.

[0174] Examples of suitable vectors systems for use with Agrobacterium are for instance binary vectors such as pBI121 and derivatives thereof co-integration vectors such as pGV1500 and derivatives of pB322. Suitable systems for transformation with denuded DNA include E. coli-vectors with high copy number, such as pUC-vectors and pBluescript II (SK+) vectors.

[0175] Upon transformation, the construct may for instance be incorporated into the genomic DNA of the plant, or it may be maintained/inherited independently in the plant (cell).

[0176] In a firer aspect, the invention therefore comprises a method in which a plant, plant cell or plant material is transformed with a genetic construct as described above.

[0177] This method may also comprise cultivating the transformed plant cell or plant material into a mature plant, and may also comprise sexually or asexually reproducing or multiplying the transformed plant (and/or the mature plant obtained from the t formed plant cell or plant material).

[0178] The invention therefore also relates to a plant, plant cell or plant material, that has been transformed with—or more generally contains—a genetic construct as described above, Preferably, such a plant, plant cell or such plant material is resistant against infection with CGMMV as described herein.

[0179] The invention furthermore relates to cultivation material such as seed, tubers, roots, stalks, seedlings etc. for such a plant, as well as descendants of such a plant, obtained through sexual or asexual reproduction techniques. Such cultivation material and/or descendants most preferably still contain or have inherited the genetic construct of the invention, and more preferably also are resistant against infection with CGMMV as described herein.

[0180] The invention will now be illustrate by means of the following non-limiting Experimental Part and by means of the Figure in which:

[0181]FIG. 1 is a schematic representation of the genome of CGMMV,

[0182]FIG. 2 gives a phylogenetic tree of COG coat protein (up) for CGMMV-SH and the ten European isolates, using the method of J. Hein with weighed residue table.

[0183]FIGS. 3-10 show examples of some preferred genetic constructs of the invention, i.e. those listed in Table 6 below.

[0184] Also, in the Experimetal Part hereinbelow, enzymes, kits, etc. were usually used according to the instructions of the manufacturer and/or using well-established protocols, unless indicated otherwise.

[0185] Experimental Part

EXAMPLE I Cloning of the Coat Protein Genes of 10 CGMMV-Isolates

[0186] 1. Collecting CGMMV Isolate

[0187] To make use of coat protein-mediated protection (CPMP) strategy against CGMMV, it is necessary to clone the coat protein cistrons of the isolates, that are economically important As the only sequence information available for CGMMV is derived from watermelon straws from the Far East, it was first decided to collect CGMMV isolates of important cucumber culture areas in Europe and the Mediterranean area. Table 1 lists the isolates collected from various geographical areas. All isolates were propagated on cucumber, and infected leaf material was stored at −80° C. The symptoms obtained after infection of cucumber cv. Hokus are listed in Table 1.

[0188] 2. Design of PCR Primers

[0189] The possibility of sequence divergence among the various collected isolates, and between the isolates and the published sequences of CGMMV-SH and CGMMV-W exists. In order to identify nucleotide regions with a high degree of sequence conservation, that could serve as a basis of PCR primer design an alignment study was carried out on corresponding sequences of CGMMV-SH, CGMMV-W and of some other related members of the tobamovirus group: Sunn-Hemp Mosaic Virus (SHMV, a variant of TMV) and Pepper Mild Mottle Virus (PMMV). For this purposes a region of 800 nucleotides just 5′ of the coat protein cistron and a region of 170 nucleotides forming the far 3′ of the viral genome were compared. In this sequence alignment, region with sufficient sequence homology among all compared viruses were identified. Based on these sequences, sets of PCR primers were designed, which are listed in Table 2. TABLE 2 Design of primers for the RT-PCR amplification of coat protein sequences of CGMMV-isolates. position on CGMMV- Primers Sequence SH sequence 5′ primers 97G01 AGGTGTCAGTGGAGAACTCATTGA 5004 97G02 GGCGTTGTGGTTTGTGG 5210 97G03 CTGTAGGGGTGGTGCTACTGT 5248 3′ primer 97G18 GCCCATAGAAACTTCAACGTC 6370

[0190] 3. Amplification of the Coat Protein Regions

[0191] From leaf meal of cucumber plants infected with each of the 11 isolate described in Table 1, a total RNA extraction was prepared Using each of the 5′ primers listed in Table 2 in combination with 3′ primer 97G18, reverse transcription of RNA and PCR amplification of cDNA with an annealing temperature of 55° C. was established using a kit manufactured by Perky Elmer Cetus. Especially in the reactions with th 5′ primer 97G03 amplification products of the correct size were obtained for each of the 11 RNA samples The PCR amplification products were directly cloned in T/A cloning vector pCR2.1 and introduced in E. coli stain NVαF′. For each of the RNA samples, the correct he of the cloned product (1.12 kb) was verified, and the clones were stored at −80° C. The amplification products of CGMMV-isolates 1 to 10 cloned in pCR2.1 were designated pKG4301 to pKG4301, and the one of CGMMV-SH cloned in pCR2.1 was designated pKG4311.

[0192] 4. Nucleotide Sequence Analysis of the Coat Protein Cistrons

[0193] The sequences of the complete inserts of the plasmids pKG4301 to pKG4310 were determined by reading in both directions using m13 forward en m13 reverse sequencing primers. The sequence of the insert of pKG4311 was already known, as contains plasmid contains a cDNA fragment of CGMMV-SH.

[0194] Sequence analysis confimred, that in each case indeed the correct cDNA fragment of CGMMV had been obtained and cloned. With one exception, each amplified and cloned cDNA fragment consisted of 1123 base pairs, containing the CGMMV coat protein in and a large part of the CGMMV movement protein cistron.

[0195] The cloned sequences of all collected European isolates (isolates 1 to 10) are approximately 97% homologous among each other, but differ on average by 10% from the published sequence of CGMMV-SH. Comparison of each individual sequence revealed, that isolates 1 and 2, both from Eastern Europe are extremely alike. The same very high degree of identity was found between both isolates from cucumber greenhouses in the Netherlands (isolates 4 and 5) and between both isolates obtained from the Almeria area in Spain (isolates 9 and 10). None of the cDNA sequences was 100% identical to any of the other ones, but the differences in sequence are no more than a few nucleotides, and sometimes only one nucleotide in the coding region of the coat protein cistron. The Japanese isolate CGMMV-SH is clearly different from any of the European isolates.

[0196] 5. Coat Protein Amino Acid Sequence Analysis

[0197] Based on the nucleotide sequences of the Open Reading Frames (ORF) of the coat protein cistrons of the 10 isolates, the to acid sequence could be deduced. In each of the analyzed sequences, the ORF consisted of a region of 486 nucleotides, coding for a protein of 161 amino acid residues. The predicted molecular mass of this proton is 17.3 kD, corresponding to earlier published results. The homology among the predicted protein sequences of the various isolates is as high as 98.1%. The only deviations are found for amino acid residue 19 (usually valine), residue 65 (mostly serine) and residue 84 (mostly leucine)

[0198] The sequence of the coat protein of the Japanese isolate CGMMV-SH only differs by 1 amino acid (residue 65) from the consensus sequence.

EXAMPLE II Cloning of the Replicase Gene of CGMMV

[0199] 1. Strategy for Replicase-Mediated Protection

[0200] By way of example, two approaches to replicase-mediated protection (RMP) against virus infections in plants were investigated.

[0201] One approach makes use of defective replicase genes in the form of truncated Open Reading Frames (ORF), in which the sequence downstream from the GDD motif had been truncated or altered through mutation.

[0202] The other approach makes use of the expression of the ‘read-through’ part of the replicase gene, i,e. the 57 kD sequence. It is thought that this ORF is not translated in the plant cell, but forms part of a larger ‘read-through’ ORF combining the coding regions of both the 129 kD replicase gene and the putative 57 kD protein gene, resulting a protein of 189 kD. However, expressing merely the 57 kD protein ORF in plant cells may result in a extremely strong resistance to infection by both virus particles and viral RNA wich also would be capable of resisting high temperatures, as well as high inoculum concentrations.

[0203] For either of these approaches, either the full-length CGMMV replicase gene must be cloned, or both constituting parts must be cloned separately. 2. Design of Primers

[0204] Because of the high sequence homology of the coat protein genes of 11 CCMMV isolates it was assumed, that the sequences of the replicase genes of the various isolates would be also highly conserved. Based on the complete sequence of the CGMMV isolate, primers were designed for the PCR amplification of the 57 kD ORF and of the 129 kD ORF (Tables 3 and 4). The primers were designed such, that they contain restriction sites for the future cloning of the amplification products. The 5′ primers contain an NcoI-site positioned such, that it will coincide with the ATG start codon of the amplified ORF. The 3′ primers contain a SacI-site downstream from the stop codon. TABLE 3 Design of primers for the LR-RT-PCR amplification of the 57 kD replicase sequence of CGMMV. position on CGMMV-SH Primers sequence sequence 5′ primer 98A88 CCATGGAGAATTCGCTGTATGTCC 3497 3′ primer 98A86 CGAGCTCTCGACTGACACCTTAC 5001

[0205] TABLE 4 Design of primers for the LR-RT-PCR amplification of the 129 kD replicase gene sequence of CGMMV. position on CGMMV-SH Primers sequence sequence 5′ primers 98A84 CCATGGCAAACATTAATGAAC 59 98A85 CAACCATGGCAAACATTAATG 56 3′ primer 98G63 TAACAGGGAGGAAAATATTACG —

[0206] 3. Long-Range Reverse Transcriptase Polymerase Chain Reactions

[0207] From the known sequence of CGMMV it was derived that the size of the 57 kD protein gene is 1.5 kb. Such a size is a the limit of the size image that can be amplified in a PCR with standard Taq polymerase. For the amplification of this cDNA fragment, and certainly for the amplification of the cDNA fragment for the 129 kD replicase gene, a different polymerase suitable for long range amplifications must be used. In these experiments, rTth DNA polymerase was used.

[0208] For direct amplification of cDNA fragments from total RNA extractions a RT-PCR kit is normally employed, combining in one reaction the activity of the Reverse Transcriptase (RT), producing a single cDNA strand complementary to the RNA template stand be at one primer annealed to the 3′ end of the RNA molecules, and the activity of the Polymerase, amplifying the thus produced single stranded cDNA molecule in a normal PCR fashion.

[0209] Because of the need to use long range polymerase, it was attempted to combine the RT with the long range polymerase to produce in one reaction large-size amplification products directly from total RNA extracts. This type of reaction was called a Long Range Reverse Transcriptase Polymerase Chain Reaction (LR-RT-PCR).

[0210] 4. LR-RT-PCR Amplification and Cloning of the 57 kD Protein Gene

[0211] Using the primers listed in Table 3 and the LR-RT-PCR described above, a specific 1.5 kb amplification product was obtained from total RNA extracts of cucumber leaves infected with CGMMV-4. This isolate was chosen, as it originated from the Dutch cucumber greenhouse cultures, and would thus represent an economically important isolate. Because long range polymerases contain a ‘proof reading’ activity and do not leave A-additions on the amplification products, as does the Taq polymerase normally employed in PCR, direct cloning of the amplification products in a TA vector accommodating the Additions W not possible. Therefore, the amplification products were briefly treated with Taq polymerase, resulting in the addition of A-overhangs on the amplified DNA molecules. These molecules could then sly be cloned in the TA vector pCR2.1, and transformed to E. coli MC1061. Clones with the correct insert size of 1.5 kb were stored at −80° C. and are known as pKG4321.

[0212] 5. Sequence Analysis of the 57 kD Protein Gene

[0213] The nucleotide sequence of the cloned insert of pKG4321 was determined by double stranded sequencing using m13 forward en m13 reuse primers and subsequent primer walking steps. The ORF coding for a putative 57 kD protein gene (SEQ ID no 3) showed 90% homology at the nucleotide level to the corresponding sequence of the papas isolate CGMMV-SH (SEQ ID no 19). The predicted amino acid sequence (SEQ ED no 4) shows a 98.2% homology to the one predicted by the CGMV-SH sequence (SEQ ID no 20).

[0214] The GDD motif characteristic for viral replicase genes resides at amino acid residues 364-366.

[0215] 6. LR-RT-PCR Amplification and Cloning of the 129 kD Replicase Gene

[0216] Using the primers listed in Table 4 in a Long Rage Reverse Transcriptase Polymerase Chain Reaction as described under 3, one specific amplification product of 3.5 kb representing the viral 129 kD replicase gene was obtained from total RNA of cucumber leaves infected with CGMMV isolate 4 (Table 1). Because long range polymerases contain a ‘proof reading’ activity and do not leave A-additions on the amplification products, as does the Taq polymerase normally employed in PCR, direct clot of the amplification products in a TA vector accommodating the A-additions was not possible. Therefore, the ampliflication products were briefly treated with Taq polymerase, resulting in the addition of A-overhangs on the amplified DNA molecules. These molecules could easily be cloned in the TA vector pCR2.1, and transformed to E. coli MC1061. Clones with the correct insert size of 3.5 kb were stored at −80° C. and are known as pKG4322.

[0217] 7. Sequence Analysis of the 129 kD Protein Gene

[0218] The nucleotide sequence of the amplification product cloned in pKG4322 was determined by double-sided sequencing using m13 forward en m13 reverse primers, and a primer walking strategy. The ORF coding for the 129 kD replicase gene (SEQ ID no 1) showed 88% homology at the nucleotide level to the corresponding sequence of the Japanese isolate CGMMV-SH (SEQ ID no 17). The ORF of the Dutch cucumber greenhouse isolate codes for a replicase protein of 1144 amino acids, which is one amino acid in extra in comparison to the CGMMV-SH strain. The predicted amino acid sequence (SEQ ID no. 2) shows a 97.1% homology to the one preited by the CGMMV-SH sequence (SEQ ID no 18).

[0219] Two GDD motifs are found at amino acid residues 256258 and 540-542.

[0220] 8. Site-Directed Mutagenesis of the 129 kD ORF

[0221] As explained above, one approach to obtain RMP in plant cells was to make use of replicase genes truncated either in the GDD motif, or truncated in the P-loop of the helicase domain. In order to create gene compression cassettes ca g such Vacated genes, a site-directed mutagenesis approach was followed to introduce stop codons at the required positions in the ORF. To this end, several parts of the 129 kD replicase ORF were re-amplified from pKG4322 as a template using specifically designed primers that included unique restriction sites for future re-assembling of the thus amplified products, as well as the required mutations in the form of stop codons (Table 5). These stop codons should ensure the proper truncation of the translation of the protein. Several stop codons were designed one after the other in the three reading frames in these primers, thus ensuring an effective translation-deficient mutation. TABLE 5 Design of primers for the site-directed mutagenesis of the 129 kD replicase gene of CGMMV. Primers sequence 98L99 GAGCTCGGATCCACTAGTAACGGC 98L107 TAGAGCTCTTGAAGCTAAGCAAATTCCG 98L108 TTCAAGAGCTCTAATCACCGAAGACAAAGGC 98L102 GAATTATATCGATTATCTATCGGC 98L103 GATAATCGATATAATTCTTCATCTGCC 98L104 AACTAGTAATTGATGATCTGTTCAAGAAG 98L105 AATTACTAGTTTCCGGAAGCAAGCAGCTCAG 98L106 GCCCTCTAGATGCATGCTCGAG

[0222] Using primers 98L103 and98L104, a fragment from the downstream half of the 129 kD gene from the GDD motif up to the ClaI-site was amplified, while simultaneously stop codons were introduced at the site of the GDD motif. This fragment cloned in TA vector pCR2.1 was called pKG4325.

[0223] Using primers 98L105 and 98L106, a fragment corresponding to the 5′ half of the 129 kD gene up to the GDD motif was amplified, while simultaneously a stop codon was introduced at the site of the GDD motif. This fragment cloned in T/A vector pCR2.1 was called pKG4326.

[0224] Replacing an XbaI-ClaI fragment of pKG4322 with the combined amplified products of pKG4325 and pKG4326 reconstitutes the full-length 129 kD replicase ORF of pKG322 with stop codons introduced at the site of the GDD motif. This construct is named pKG 4329.

[0225] Using primers 98L99 and 98L107, a fragment at the far downstream end of the 129 kD gene from the P-loop to the end of the ORF was amplified, while simultaneously stop codons were introduced at the site of the P-loop. This fragment cloned in T/A vector pCR2.1 was called pKG4327.

[0226] Using priers 98L108 and 98L102, a fragment corresponding to a central part of the 129 kD gene from the GDD motif up to the P-loop was amplified, while simultaneously a stop codon was introduced at the site of the P-loop. This fragment cloned in T/A vector pCR2.1 was called pKG4328.

[0227] Replacing an BamHI-ClaI fragment of pKG4322 with the combined amplified products of pKG4327 and pKG4328 reconstitutes the fullength 129 kD replicase ORF of pKG4322 with stop codons introduced at the site of the P-loop. This construct is named pKG4330.

EXAMPLE III Transformation of Cucumber

[0228] 1. Construction of a CGMMV-Leader Sequence

[0229] For optical expression and stability of the replicase gene transcripts in plant cells, it was thought necessary to add a sequence identical to the 5′ untranslated (5′ UTR) region of the CGMMV genome upstream from the ORF sequence in the plant expression cassette. Because the 5′ UTR of viral genomes contain highly repetitive RNA, this sequence could not be obtained by RT-PCR amplification, as no specific primers could be designed. Instead, a synthetic region identical to the 5′ UTR of CGMMV-SH was assembled from the four oligonucleotide sequences: 97G40 (CTAGAGTTTTAATTTTTATAATTAAACAAA), 97G41 (TCAAAATTAAAAATATTAATTTGTTTGTTGTTGTTG), 97G42 (CAACAACAACAACAACAAACAATTTTAAAACAACAC) and 97G43 (TTGTTGTTTGTTAAAATTTTGTTGTGGTAC).

[0230] These oligonucleotides were designed such, that outside the sequence corresponding to the 5′ UTR they contain restriction sites for XbaI and NcoI, thus facilitating further cloning. Adding the four oligonucleotides together will cause spontaneous assembling due to the design of extensive regions of overhang. Using these restriction sites, the assembled mixture was cloned in a plant expression vector containing an Arabidopsis thaliana plastocyanine promoter (Vorst et al, 1993) and a Agrobacterium tumefaciens nopaline synthase terminator sequence (Depicker et al., 1982) in a pUC19-derived plasmid. This expression cassette was called pKG1315. The complete expression cassette consisting of the plastocyanine promoter, the CGMMV leader sequence and the nos terminator was subsequently removed from pKG1315 using HindIII and EcoRI as restriction enzymes, and recloned in the corresponding restriction sites of:

[0231] 1) an intermediate type Agrobacterium transformation vector for cointegrate type vector systems containing an nptII selectable marker gene cassette to create pKG1575, and

[0232] 2) an intermediate type Agrobacterium transformation vector for cointegrate type vector systems containing no selectable marker gene to create pKG1110.

[0233] 2. Construction of Transformation Vectors

[0234] The three cloned and modified replicase constructs of pKG4321, pKG4329 and pKG4330 were isolated from the plasmids by restriction with BamHI (filled in with Klenow) and NcoI and ligated into the SacI (filled in with Klenow) and NcoI sites of each of the two transformation vectors pKG1575 and pKG1110, resulting in a total of six transformation vectors, listed in Table 6. TABLE 6 List of six transformation vectors for the expression in plants of parts of the CGMMV-replicase gene. Vector vector type modified CGMMV-replicase gene PKG4331 Intermediate type with nptII  57 kD ORF PKG4332 intermediate type with nptII 129 kD ORF with stopcodon in GDD motif PKG4333 intermedinte type with nptII 129 kD ORF with stopcodon in P-loop PKG4334 intermediate type  57 kD ORF PKG4335 intermediate type 129 kD ORF with stopcodon in GDD motif PKG4336 intermediate type 129 kD ORF with stopcodon in P-loop

[0235] 3. Transformation of Cucumber

[0236] The intermediate type transformation vectors pKG4331 and pKG4333 were introduced into Agrobacterium tumefaciens strain GV2260 by tri-parental mating. Transconjugants which had incorporated the intermediate type vector into their Ti-plasmids through homologous recombination were selected on the basis of streptomycin and spectinomycin resistance and analyzed for the correct insertion of the vector.

[0237] Cucumber plants were transformed with these two strains of Agrobacterium, as well as wit an Agrobacterium strain harbouring only the nptII selection marker, using published procedures. A number of transgenic cucumber plant were obtained. The plants were transferred to a greenhouse to flower and set seed, The seedlings germinating from these R1 seed were mechanically infected with CGMMV isolate 1-3 weeks post-inoculation, the plants were scored for symptoms of virus infection, as described in the assay for tolerance to virus infection set out in under 4, below,

[0238] 4. Assay for Tolerance to Virus Infection

[0239] The seedlings of transgenic cucumber germinating from these R1 seed were mechanically infected with CGMMV isolate 1. Fresh inoculum was prepared from a crude leaf extract of susceptible non-transgenic cucumber plants cv. Hokus pre-infected with this same isolate 3 weeks previously. Seedlings of non-transformed cucumber plants were used as controls in the assay. During 21 days post-inoculation the appearance of viral symptoms was scored visually every 2 days. In this assay, individual plants are scored as being tolerant when they remain free of visible symptoms for at least 7 days, and preferably more than 14 days, and more preferably more than 21 days post-inoculation.

[0240] Sixty-four independent transgenic lines were assayed, with 14 to 20 seedlings for each line. Control seedlings all became diseased within 9 days post-inoculation. A number of seedlings in seventeen of the transgenic lines showed clear absence of symptoms for a prolonged period of time, and r ed free of symptoms after 21 days post-inoculation. Of some transgenic lines, the number of symptom-fee plants corresponded to Mendelian segregation of a tansgenic present in a single locus. In one particular transgenic cucumber line 4 out of 14 seedlings remained symptom-free during the assay period, which may indicate that the tolerant phenotype corresponds to the homozygous state of a transgene present in one single locus, although, as mentioned above, the invention is not limited to a specific mechanism.

EXAMPLE IV

[0241] 1. Construction of Hairpin RNA Construct

[0242] 1.1. Genome Organization of CGMMV

[0243] The genome of CGMMV consists of a single-stranded RNA molecule coding for a 129 kD protein with replicase function (RNA dependent RNA polymerase), a putative 54 kD protein, a 29 kD movement protein and a 17.3 kD coat protein The presence of the 54 kD protein has not been detected in infected plants. However, a 186 kD protein has been found instead, being the product of a read-through translation of the 129 kD and the 54 kD Open Reading Frames. The 186 kD protein is also thought to play a role in virus replication. The genome structure of CGMMV is thus very similar to those of other members of the tobamovirus group.

[0244] The complete sequence of only one isolate of CGMMV has been determined (Ugaki et al., 1991; Genbank accession numbers D12505 and D01188). This isolate “SH” had been found infected watermelon plants i East Asia Furthermore, the sequence of the coat protein gene of one other isolate (“W”) obtained from infected watermelon is known (Meshi et al., 1983; Genbank accession numbers V01551 and J02054), as well as the sequence of the 29 kD movement protein gene of a watermelon strain (Saito et al, 1988; Genbank accession number J04332). The nucleotide sequence of the CGMMV-SH isolate shows 55 to 56% identity with tobacco mosaic virus (TMV) and tobacco mild green mosaic virus (TMGMV), both other members of the tobamovirus group (Ugaki et al., 1991).

[0245] 1.2. Cloning of the RdRp Gene of CGMMV

[0246] In the present example of the invention, the sequence elected for constructing the constructs is the RNA dependent RNA polymerase of CGMMV.

[0247] a. Primer Design

[0248] Because of the high sequence homology of the coat protein genes of 11 CGMMV isolates it was assumed, that the sequences of the replicase genes of the various isolates would be also highly conserved. Based on the complete sequence of the CGMMV-SH isolate, primers were designed for the PCR amplification of the 54 kD ORF and of the 129 kD ORF (Tables 7 and 8). The primers were designed such, that t contain restriction sites for the future cloning of the amplification products. The 5′ primers contain an NcoI-site positioned such, that it will coincide with the ATG start codon of the amplified ORF. The 3′ primers contain a SacI-site downstream from the stop codon. TABLE 7 Design of primers for the LR-RT-PCR amplification of the 54 kD replicase sequence of CGMMV. position on CGMMV-SH primers sequence sequence 5′ primer 98A88 CCATGGAGAATTCGCTGTATGTCC 3497 3′ primer 98A86 CGAGCTCTCGACTGACACCTTAC 5001

[0249] TABLE 8 Design of primers for the LR-RT-PCR amplification of the 129 kD replicase gene sequence of CGMMV. position on CGMMV-SH primers sequence sequence 5′ primers 98A84 CCATGGCAAACATTAATGAAC 59 98A85 CAACCATGGCAAACATTAATG 56 3′ primer 98G63 TAACAGGGAGGAAAATATTAC

[0250] b. Long-Range Reverse Transcriptase Polymerase Chain Reactions

[0251] From the known sequence of CGMMV-SH it was clear, that the size of the 54 kD protein gene is 1.5 kb. Such a size is at the limit of the size range that cam be amplified in a PCR with standard Taq polymerase. For the amplification of this cDNA fragment, and certainly for the amplification of the cDNA fragment for the 129 kD replicase gene, a different polymerase suitable for long range amplifications must be used. In these experiments, a long-range polymerase was used.

[0252] For direct amplification of cDNA fragments from total RNA extractions a RT-PCR kit is normally employed, combining one reaction the activity of the Reverse Transcriptase (RT), producing a single cDNA strand complementary to the RNA template strand beginning at one primer annealed to the 3′ end of the RNA molecules, and the activity of the Polymerase, amplifying the thus produced single stranded cDNA molecule in a normal PCR fashion.

[0253] Because of the need to use long range polymerase, it was attempted to combine the RT with the long range polymerase to produce in one reaction large-size amplification products directly from total RNA extracts. This type of reaction was called a Long Range Reverse Transcriptase Polymerase Chain Reaction LR-RT-PCR).

[0254] c. LR-RT-PCR Amplification and Cloning of the 54 kD Protein Gene

[0255] Using the primers listed in Table 1 and the LR-RT-PCR described above, a specific 1.5 kb amplification product was obtained from total RNA extracts of cucumber leaves infected with CGMMV-4. This isolate was chosen, as it originated from the Dutch cucumber greenhouse cultures, and would thus represent an economically important isolate. Because long range polymerases contain a ‘proof reading’ activity and do not leave A-additions on the amplification products, as does the Taq polymerase normally employed in PCR, direct cloning of the amplification products in a T/A vector accomodating the A-additions was not possible. Therefore, the amplification products were briefly treated with Taq polymerase, resulting in the addition of A-overhangs on the amplified DNA molecules. These molecules could then easily be cloned in the T/A vector pCR2.1, and transformed to E. coli MC1061. Clones with the correct insert size of 1.5 kb were stored at −80° C. and are known as pKG4321.

[0256] d. Sequence Analysis of the 54 kD Protein Gene

[0257] The nucleotide sequence of the cloned insert of pKG4321 was determined by double-stranded sequencing using m13 forward en m13 reverse primers. The ORF coding for a putative 54 kD protein gene showed 90% homology at the nucleotide level to the corresponding sequence of the Japanse isolate CGMMV-SH. The predicted amino acid sequence shows a 98.2% homology to the one predicted by the CGMMV-SH sequence.

[0258] The GDD motif characteristic for viral replicase genes resides at amino acid residues 364-366.

[0259] e. LR-RT-PCR Amplification and Cloning of the 129 kD Replicase Gene

[0260] Using the primers listed in Table 9 in a Long Range Reverse Transcriptase Polymerase Chain Reaction as described in 6.2.3, one specific amplification product of 3.5 kb representing the viral 129 kD replicase gene was obtained from total RNA of cucumber leaves infected with CGMMV isolate 4 (Table 1). Because long range polymerases contain a ‘proof reading’ activity and do not leave A-additions on the amplification products, as does the Taq polymerase normally employed in PCR, direct cloning of the amplification products in a T/A vector accomodating the A-additions was not possible. Therefore, the amplification products were briefly treated with Taq polymerase, resulting in the addition of A-overhangs on the amplified DNA molecules. These molecules could easily be cloned in the T/A vector pCR2.1, and transformed to E. coli MC1061. Clones with the correct insert size of 3.5 kb were stored at −80° C. and are known as pKG4322. TABLE 9 Design of primers for the PCR amplification of CGMMV target sequences and plant intron sequences, to be assembled in hairpin encoding gene constructs. restriction site Primer target added sequence primer 1 5′ RdRp SacI CGAGCTCATCTCGTTAGTCAGC primer 2 3′ RdRp BamHI GGGATCCACGTCTGGACAGG primer 3 5′ RdRp XbaI CTCTAGAATCTCGTTAGTCAGC primer 4 3′ RdRp BamHI AGGATCCTACACGAACCTATC primer 5 5′ AO3 BamHI AGGATCCATTGCGGTAACACAAC primer 6 5′ AO3 BglII TAGATCTATTGCGGTAACACAAC primer 7 3′ AO3 BglII TAGATCTGTGTGATTCTGG primer 8 3′ AO3 BamHI AGGATCCGTGTGATTCTGG primer 9 5′ IV2 BamHI AGGATCCGTGTACGTAAGTTTC primer 10 5′ IV2 BglII TAGATCTGTGTACGTAAGTTTC primer 11 3′ IV2 BglII TAGATCTGTGATACCTGCAG primer 12 3′ IV2 BamHI AGGATCCGTGATACCTGCAG primer 13 5′ RdRp SacI CGAGCTCATCTCGTTAGTCAGCTAGC primer 14 3′ RdRp BamHI AGGATCCTTTGTGCCTCTGTACATG primer 15 5′ RdRp XbaI CTCTAGAATCTCGTTAGTCAGCTAGC primer 16 3′ RdRp BamHI AGGATCCATCAACCCTAAATTGAGCC primer 17 5′ RdRp BamHI AGGATCCAGCAGGGAAATAAGTACGC primer 18 3′ RdRp BamHI AGGATCCGGTATGGACAAAATCAGC primer 19 5′ AO3 BamHI AGGATCCATTGCGGTAACACAACCTCTC primer 20 3′ AO3 BglII TAGATCTGTGTGATTCTGGAAAAG primer 21 3′ IV2 BglII TAGATCTGTGATACCTGCACATCAAC primer 22 5′ IV2 BamHI AGGATCCGTGTACGTAAGTTTCTGCTTC primer 23 5′ RdRp XbaI CTCTAGAATCTCGTTAGTCAGCTAGC primer 24 3′ RdRp BamHI AGGATCCAGCAGGGAAATAAGTACGC

[0261] f. Sequence Analysis of the 129 kD Protein Gene

[0262] The nucleotide sequence of the amplification product cloned in pKG4322 was determined by double-stranded sequencing using m13 forward en m13 reverse primers, and a primer walking strategy. The ORF coding for the 129 kD replicase gene showed 88% homology at the nucleotide level to the correponding sequence of the Japanse isolate CGMMV-SH. The ORF of the Dutch cucumber greenhouse isolate codes for a replicase protein of 1144 amino acids, which is one amino acid in extra in comparison to the CGMMV-SH. The predicted amino acid sequence shows a 97.1% homology to the one predicted by the CGMMV-SH sequence.

[0263] 1.3. Cloning of Target Sequences

[0264] In one particular example of the invention, a fragment of 489 nt of the 5′ end of RdRP gene of CGMMV was chosen as a target sequence for the construction of sense and antisense sequences separated by a stuufer fragment. These fragments were isolated from the cloned 129 kD ORF of pKG4322 (described above) by PCR amplification PCR primers were designed a corresponded to the 5′ and 3′ parts of the chosen target sequence, and included in the 5′ part of the primer sequences, an additional restriction site to facilitate the cloning of the amplification products.

[0265] One primer set (primer 1 and primer 2, Table 9) was designed to amplified the chosen target fragment of 489 bp from pKG4322, whereby restriction sites for SacI (primer 1) and BamHI (primer 2) were introduced by the PCR process at either end of the fragment.

[0266] A second primer set (prier 3 and primer 4, Table 9) was designed to amplify from pKG4322 the same target sequence of 489 bp from pKG4322 plus an additional sequence of 332 bp downstream of the target sequence in the CGMMV RdRP gene. Prier 4 and primer 5 added restriction sites for XbaI and BamHI, respectively, at either end of the amplified fragment. Details of the priers are given in Table 9. The PCR products obtained by amplification of the target sequences using the respective primers were cloned in T/A cloning vector pCR2.1, resulting in pCG1 (489 bp target sequence) and pCG2 (821 bp fragment). The ligation product was transformed to E. coli MC1061 and stored at −80° C. The sequences of the cloned PCR products in pCG1 and pCG2 were verified by sequence analysis and found to correspond exactly to the sequence of the template DNA of pKG4322.

[0267] In a similar way, one fragment of the target sequence was obtained by PCR on template pKG4322 DNA using primers 13 and 14, which resulted in a 398 bp amplification product with restriction sites for BamHI and SacI on either end. The second fragment of the target sequence was obtained on pKG4322 DNA as template with primers 15 and 16, resulting in an amplification product of 698 bp, of which the first 398 bp were identical to the fragment obtained with primers 13 and 14 and which extended another 300 bp in the 3′ direction. This product contained restriction sites for BamHI and XaI on either end. Both fragments were cloned in T/A cloning vector pCR2.1 to create plasmids pKG4347 and pKG4349, respectively.

[0268] Yet another set of amplification reactions was designed to obtain larger fragments of the target sequence. In a similar way as described above, one 805 bp PCR product of the target sequence was obtained with primers 13 and 17 with restriction sites fob SacI and BamHI on either end, and a second 1102 bp product was o ed with primers 15 and 18 and contained restriction sites for BamHI and XbaI on either end. The sequence of the first 805 bp of the second PCR product was identical to the sequence of the first PCR product, while the second product extended for another 297 bp in the 3′ direction. Both fragments were cloned in T/A cloning vector pCR2.1 to create plasmids pKG4351 and pKG4346, respectively.

[0269] 1.4. Construction of Hairpin RNA Encoding Transformation Vectors

[0270] The restriction sites on the ends of the amplified target sequences allowed the simultaneous cloning of both fragments by a three-way ligation in a suitable transformation vector such as pKG1572. This information vector is a cointegrate type T-DNA vector for Agrobacterium-mediated transformation of plants, carrying between the T-DNA borders a) the plant selectable marker gene nptII driven by a nos promoter, b) a CaMV 35S promoter for constitutive expression in plants, c) a multiple cloning site, and d) the nos polyadenylation sequence (FIG. 9). Furthermore, this vector contain a backbone sequence homologous to pBR322, including tie ColE1 origin of replication for maintence in E. coli, and the aadA selectable marker gene for bacterial resistance to streptomycin and spectinomycin.

[0271] The presence of the restriction sites for BamHI at both 3′ ends of the PCR products allowed the insertion of both fragments in reverse orientation to each other in the cloning vector. Thus, a construct was created, that included the target sequence of 489 bp in reverse orientation, separated by a ‘stuffer’ fragment of 332 bp, that was included in the amplification product generated with primers 3 and 4, This ‘stuffer’ fragment is included to guarantee stability of the inverted repeat sequences in E. coli. The construct obtained by the three-way ligation was named pCG3 and was transformed to E. coli MC1061 and stored at −80° C. The pCG3 can construct was verified by sequence analysis.

[0272] In a similar way, the cloned PCR products of pKG4347 and pKG4349 were inserted in transformation vector pKG1572 in a 3-way ligation, resulting in inverted repeat orientation of the 398 bp identical parts of the products, separated by a 300 bp ‘stuffer’ sequence. The resulting transformation vector was named pKG4359 (FIG. 11).

[0273] Similarly, the PCR products of pKG4351 and pKG4346 were inserted in a 3-way ligation in transformation vector pKG1572 to create pKG4358 (FIG. 12), consisting of 805 bp inverted repeats of the CGMMV target sequence, separated by a 297 bp ‘stuffer’. All constructs were transformed to E. coli MC1061 and stored at −80° C.

[0274] 1.5. Transformation of Cucumber

[0275] Transformation vector pCG3 was subsequently transferred to the disarmed Agrobacterium tumefaciens strain GV2260 by tri-parental mating. Strain GV2260 carries in its Ti-plasmid pGV2260 a 3.8 kb sequence of pBR322, homologous to a similar fragment of pBR322 residing in the backbone of the cointegrate transformation vectors such as pKG1572 and pCG3. This homologous sequence allows the stable integration of the transformation vector into the Ti-plasmid by homologous recombination.

[0276]Agrobactrium colonies were grown and subcultured on streptomycin end spectinomycin to select for the presence of the integrated transformation vector. Selected colonies were subjected to Southern blot analysis with the aadA selectable marker gene present on the cointegrate vector as a probe to verify single integration events in the Ti-plasmid Furthermore, the Agrobacterium colonies were subjected to PCR analysis using primer sets capable of amplifying overlapping fragments covering the entire T-DNA of the integrated transformation vector to verify the correct integration in the Ti-plasmid of the complete T-DNA. A number of Agrobacterium colonies verified in this way were named GV2260 (pGV2260::pCG3) and were stored at −80° C.

[0277] In a similar way, the transformation vectors pKG4358 and pKG4359 were transferred to Agrobacterium GV2260. These were named GV2260 (pGV2260::pKG4358) and GV2260 (pGV2260::pKG4359), respectively.

[0278] The hairpin RNA encoding constructs are introduced into the genomes of cucumber plants using Agrobacterium-mediated transformation procedures known i the art. Briefly, cotyledon explants of young cucumber seedings germinated in vitro are inoculated with a suspension of an Agrobacterium strain containing any one of the previously described transformation constructs integrated on their Ti-plasmids. The explants, after 1 to 5 days of cocultivation with Agrobacterium, are transferred to Petri dishes with regeneration medium containing, in addition to minerals, vitamins, sugars and plant growth regulators, kanamycin sulphate in concentrations of 50 to 300 mg/l as a selective aged, and incubated in growth chambers under the appropriate temperature and light conditions for the specific cucumber cultivar under study.. The cotyledon explants will, in the course of the following weeks, produce primordia, that grow out to shoots. When the shoots have grown sufficiently long, the are transferred to glass jars with rooting medium containing the selective agent kanamycin sulphate. Truly transformed shoots will remain green and form roots on this medium, are ultimately hardened off transplated to soil and transferred to a greenhouse. Viral resistance assays are preferably performed on young seedlings originating from crosses between tranformed maternal cucumber plants and a pollinator line. Virus resistance assays can simply be carried out by mechanical inoculation of the seedlings with a crude extract in phosphate buffer of leaves of a severly diseased cucumber plant previously infected. The resistance phenotype is observed 21 days post-inoculation by absence of leaf chlorosis and stunted growth, which has become apparent in non-transgenic control sets. Depending on the number of independently integrated copies of the gene construct in the plant genome, the number of resistant seedlings versus the number of susceptible seedlings will correspond to a Mendelian segregation.

[0279] The resistance against virus infection obtained may be expressed as the degree of tolerance, by scoring the period in number of days post-infection which it takes for 50% of transformed seedlings in the infected population to show symptoms of virus infection in many cases, however, the resistance to CGMMV infection obtained by hairpin RNA constructs is sufficiently effective that a score of 50% of transformed seedlings showing symptoms will not be observed within a period of several months. In such case, all seedlings remaining free of symptoms 21 days post-inoculation are scored as being resistant, and the number of resistant seedlings out of the total number of infected transformed seedligs is expressed as a percentage of effectiveness of resistance. In this way, differences in the effectiveness of the various described intron-spliced hairpin RNA constructs in conferring virus resistance are evaluated.

[0280] The virus resistance assays described above can be performed using inoculations of viral isolates of different orgin. In this way, the intron-spliced hairpin RNA constructs targetted again CGMMV are shown to be effective against all isolates of CGMMV described in Table 1, including the Japansese isolate CGMMV-SH, as well as to isolates of the related cucurbit-infecting tobamoviruses Kyuri Green Mottle Mosaic Virus (KGMMV) and Cucumber Fruit Mottle Mosaic Virus (CFMMV).

EXAMPLE V

[0281] 2.1. Cloning of Plant Intron Sequences

[0282] In a second example, an alternative ‘stuffer’ fragment necessary for stable maintenance of the inverted repeat structure in E. coli is chose in this case, use is made of a plant intron sequence capable of being spliced after transcription of the inverted repeat sequence in plant cells. The publication of Smith et al. (Nature 407: 319-320, 2000) describes the use of intron 2 of the PdK gene Flaveria as a ‘stuffer’ fragment in gene silencing constructs to obtain a high degree of resistance to infections with PVY. However, this Flavenia intron is very large (1.8 kb) and the correct splicing of this intron in Cucumis plant cells is uncertain. In this example, two types of plant introns are employed, of which the correct splicing in Cucumis has been verified. The intron is the 188 bp IV2 intron of the potato LS-1 gene, that is frequently encountered in gusA reporter gene constructs to obtain expression of beta-glucuroridase in plant cells with simultaneous absence of beta glucuronidase expression in bacterial cells such as Agrobacterium tumefaciem. From experience it is known that cucumber and melon plants correctly express beta-glucuronidase from introduced gene constructs containing the gusA gene with the potato IV2 intron.

[0283] The second intron employed is the 532 bp Cucumis melo ascorbate oxidase intron AO3, which by its very nature is known to be spliced correctly in Cucumis melo (melon plants and is expected to function properly in the related species Cucumis sativus (cucumber).

[0284] Both these intron sequences were obtained by PCR amplification using primers, which, in the 5′ part of the primer sequences, include an additional restriction site to facilitate the cloning of the amplification products. Thus, melon intron AO3 was amplified from total genomic DNA of young melon seedlings using primers 5 and 7 (see Table 9), which each contains a restriction site fox BamHI or BglII, respectively, at their 5′ ends.

[0285] An alternative PCR reaction to obtain gene melon AO3 intron employed primers 19 and 20, and yielded a PCR product with 546 bp of amplified intron sequence, which corresponded to the known AO3 intron sequence, and which contained restriction sites for BamHI and BglII on either end. This PCR product was cloned in the T/A cloning vector pCR2.1 to yield plasmid pKG4355.

[0286] In order to test the effect of the cloned intron sequences in the hairpin RNA encoding gene constructs, control gene constructs were anticipate in which the intron sequences were placed in reverse orientation. To this end, a similar primer set was designed, consisting of primers 6 and 8, in which the restriction sites for BamHI and BglII were reversed as compared to primers 5 and 7 (Tabel 9). The PCR products obtained by amplification of the AO3 intron sequence using said primer sets were cloned in T/A cloning vector pCR2.1, resulting in pCG4 (BamHI-AO3 intron-BglII) and pCG5 (BglII-AO3 intron-BamHI). The sequences of the cloned PCR products were verified by sequence analysis and found to correspond exactly to the known sequences of intron.

[0287] The potato IV2 intron was amplified from the vector construct pKGT-3 carrying a gusA gene containing this intron with primes 9 and 11 (see Table 9), each carrying an additional restriction site fr BamHI and BglII, respectively. Also for this intron, an additional PCR product with BamHI and BglII at the removed positions on either side of the amplification product was using PCR primers 10 and 12 (Table 9). The PCR products thus obtained were cloned in cloning vector pCR2.1, and named pCG6 (BamHI-potato IV2 intron-BglII) and pCG7 (BglII-potato IV2 intron-BamHI).

[0288] An alternative reaction to obtain the potato IV2 intron for cloning in the correct orientation employed primers 21 and 22 in a PCR reaction on template DNA of pKG1600, a plasmid vector containing the gusA gene of this intron. The reaction yielded an amplification product with 202 bp of IV2 intron sequence, and which contained restriction sites for BamHI and BglII on either end. This PCR product was cloned in the T/A cloning vector pCR2.1 to yield plasmid pKCG4353.

[0289] 2.2. Cloning of Introns in the Hairpin RNA Encoding Expression Cassettes

[0290] The target sequence of 489 bp of the CGMMV RdRP gene was reamplified from the cloned CGMMV RdRp gene in vector pKG4322 by PCR using primer 2 and primer 3, as described in Example IV. This PCR reaction produced a fragment containing the target sequence, that was identical to the insert of pCG1 of Example IV) except that the 5′ restriction site generated at the 5′ end of the PCR product is a recognition site XbalI instead of for SacI. The PCR product was cloned in T/A vector pCR2.1 to produce pCG8. The ligation product was transformed to E. coli MC1061 and stored at −80° C. The sequences of the cloned PCR product in pCG8 was verified by sequence analysis and found to correspond exactly to the sequence of the template DNA of pKG4322.

[0291] In a similar way, the 398 bp CGMMV target sequence was reamplified from pKG4322 template DNA using primers 23 and 14 to create restriction sites for BamHI and XbaI on either end, to facilitate the cloning in intron-containing repeat constructs. This PCR fragment, after cloning in the T/A cloning vector pCR2.1, was named pKG4348.

[0292] Yet in another, similar, PCR reaction, an 806 bp CGMMV target sequence was reamplified from pKG4322 template DNA using primers 23 and 24 to create restriction sites for BamHI and XbaI on either end, to facilitate the cloning in intron-containing repeat constructs. This PCR fragment, after cloning in the T/A cling vector pCR2.1, was named pKG4350.

[0293] The vector pCG1 of Example IV was digested with restriction enzymes SacI and BamHI and the rent containing the 489 bp target sequence was isolated from gel and ligated into the transformation vector pKG1572 (described in Example IV) digested with the same two restriction enzymes. This ligation product, named pCG9, was transformed to E. coli MC1061. The correct structure of pCG9 was then verified by restriction analysis.

[0294] Next, both plant intron sequences in sense and in antisense orientations, cloned in vectors pCG4 to pCG7 were isolated from their vectors by digestion with BamHI and BglII and ligated into pCG9 digested with BamHI. The ligation products were transformed to E. coli MC1061. This cloning step placed the plant intron sequences next to the 489 bp CGMMV target sequence in the expression cassette of the transformation vector. Since restriction enzymes BanHI and BglII are isoschizomers and produce identical ‘sticky ends’, two orientations of the intron sequences were obtained in the ligation products. Colonies of all four cloning reactions were analysed by restriction enzyme digestion, and only those colonies of all four reactions were retained for further cloning, that contained the single BamHI site at a position between the in sequence and the CaMV 355 promoter. The cloning intermediates were named pCG10 (sense AO3 intron), pCG12 (sense IV2 intron), pCG14 (antisense AO3 intron) and pCG16 (antisense IV2 intron).

[0295] Subsequently, the 489 bp target sequence of pCG8 was isolated from the vector by digestion with XbaI and BamHI and ligated into the vectors pCG10, pCG12, pCG14 and pCG16, each digested with XbaI and BamHI. This Ligation step produced the final transformation vectors containing two copies of the 489 bp target sequence in reverse orientation to each other, thus encoding a hairpin RNA structure, and separated from each other by plant intron sequences in sense and antisense orientation The ligation products were named pCG11 (sense AO3 intron), pCG13 (sense IV2 intron), pCG15 (antisense AO3 intron) and pCG17 (antisense IV2 intron), and were transformed to E. coli MC1061 and stored at −80° C. The correct structure of the vectors was verified by sequence analysis,

[0296] The other cloned amplification products of target and intron sequences described in this example were assemble in the follow manner. The melon AO3 intron of pKG4355, as a BamHI-BglII fragment, and the 398 bp CGMMV RdRp target sequence of pKG4347, as a BamHI-SacI fragment, were simultaneously ligated in the transformation vector pKG1572. Subsequent insertion of a BamHI-XbaI fragment of pKG4348 into the ligation product yielded transmformation vector pKG4375 (FIG. 13), which carried inverted repeats of the 398 bp CGMMV RdRp target sequence, separated by the melon AO3 intron,

[0297] To create a similar construct with the longer CGMMV target sequences, tie melon AO3 intron of pKG4355, as a BamHI-BglII fragment, and the 805 bp CGMMV RdRp target sequence of pKG4351, as a BamHI-SacI fragment were simultaneously ligated in the transformation vector pKG1572. Subsequent insertion of a BamHI-XbaI fragment of pKG4350 into the ligation product yielded transformational vector pKG4377 (FIG. 14), which carried inverted repeats of the 805 bp CGMMV RdRp target sequence, separated by the melon AO3 intron.

[0298] Likewise, transformation vectors with CGMMV RdRp inverted repeats separated by the potato IV2 intron were created. The potato IV2 intron of pKG4353, as a BamHI-BglII fragment, and the 398 bp CGMMV RdRp target sequence of pKG4347, as a BamHI-SacI fragment, were simultaneously ligated in the transformation vector pKG1572. Subsequent insertion of a BamHI-XbaI fragment of pKG4348 into the ligation product yielded transformation vector pKG4374 (FIG. 15), which carried inverted repeats of the 398 bp CGMMV RdRp target sequence, separated by the potato IV2 intron.

[0299] Also, the potato IV2 intron of pKG4353, as a BanHI-BglII fragment, and the 805 bp CGMMV RdRp target sequence of pKG4351, as a BamHI-SacI fragment, were simultaneously ligated in the transformation vector pKG1572. Subsequent insertion of a BamHI-XbaI fragment of pKG4350 into the ligation product yielded transformation vector pKG4376 (FIG. 16), which carried inverted repeats of the 805 bp CGMMV RdRp target sequence, separated by the potato IV2 intron.

[0300] All constructs were transformed to E. coli MC1061 and stored at −80° C.

[0301] 2.3. Transformation of Cucumber

[0302] After transferred the transformation vectors to Agrobacterium tumefaciens strain GV2260 as described in Example TV, cucumber plants transformed with these Agrobacterium strains will be resistant to CGMMV infection. The preferred manner to assay virus resistance is described in Example IV. With all four gene constructs resistance to CGMMV infection is obtained. The efficacy of the intron sequences in sense orientation as opposed to constructs with introns in antisense orientation is apparent from the high percentage of cucumber lines showing extreme resistance to CGMMV infection.

[0303] Hereinabove, the invention has been described under the assumption that resistance against CGMMV is generated “at the protein level”, i.e. that the “nucleotide sequence encoding a defective variant of the replicase gene of CGMMV” codes for a “defective replicase”, the expression of which at cellular level generates the desired resistance against CGMMV. Hereinabove, the invention has been described under the assumption, that the resistance to CGMMV can also be generated at the RNA-level, e.g. down-regulation of gene expression due to RNA sequence homology. However, the invention is not limited to any explanation or mechanism, and is not particularly limited to the use of a particular type of nucleotide sequence (i.e. encoding a “defective replicase” or a “hairpin”).

[0304] References

[0305] Anderson, J. M., Palukaitis, P. and M. Zaitin (1992) A defective replicase gene induces resistance to cucumber mosaic virus in transgenic tobacco. Proc.Nat.Acad.Sci.USA 89: 8759-8763.

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[0308] Christou et al. (1992) IAPTC Newsletter 2-14.

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[0312] Goldbach, R, and P. De Haan (1993) Prospects of engineered forms of resistance against tomato spotted wilt vim. Seminars in Virology 4: 381-387.

[0313] Golemboski, D. B., G. P. Lomonosoff and M. Zaitlin (1990) Plants transformed with a tobacco mosaic virus nonstructural gene sequence are resistant to the virus. Proc. Natl. Acad. Sci.USA 87: 6311-6315.

[0314] Hollings, M., Y. Komuro and H. Tochihara (1975) Cucumber Green Mottle Mosaic Vu. C. M. I./A. A. B. Descriptions of Plant Viruses, nr. 154.

[0315] Horsch, R. B., J. G. Fry, N. L. Hoffmann, D. Eichholtz, S. G. Rogers and R. T. Fraley (1985) A simple and general method for transferring genes into plants. Science 227: 1229-1231.

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[0317] Meshi, T., R. Kiyama, T. Ohno and Y. Okada (1983) Nucleotide sequence of the coat protein cistron and the 3′ noncoding region of cucumber green mottle mosaic virus (watermelon strain) RNA. Virology 127: 54-64.

[0318] Prins et al. (1994) Molec.Plant-Microbe Interact 8: 85-91.

[0319] Ugaki M., M. Tomiyama, T. Kakutani, S. Hidaka, T. Kiguchi, R. Nagata, T. Sato, F. Motoyoshi and M. Nishiguchi (1991) The complete nucleotide sequence of Cucumber Green Mottle Mosaic Virus (SH strain) genomic RNA J.Gen.Virol. 72; 1487-1495.

[0320] Rogus, S. G., H. J. Klee, R. B. Horsch and R. T. Fraley (1986) Gene transfer in plants: production of transformed plants using Ti plasmid vectors. Meth. Enzymol. 118: 627-640.

[0321] Shillito, R. D., M. W. Saul, J. Paszkowski, M. Muller and I. Potrykus (1985) High efficiency direct gene transfer to plants. Bio/Technology 3: 1099-1103.

[0322] Vaira, A. M,, L. Semeria, S. Crespi, V. Lisa, A. Allavena and G. P. Accotto (1995) Resistance to Tosposviruses in Nicotiana benthamiana transformed with the N gene of tomato spotted wilt virus: correlation between transgene expression and protection in primary transformants. Molec.Plant-Microbe Interact. 8; 66-73.

[0323] Vorts O., P. Kock, A. lever, B. Weterings, P. Weisbeek and S. Smeekens (1993) The promoter of the Arabidopsis thaliana plastocyanin gene contains a far upstream enhancer-like element involved in chloroplast-dependent expression. Plant Journal 4:933-945.

[0324] Wilson, T. M. A. (1993) Strategies to protect crop plants against viruses: pathogen-derived resistance blossoms. Proc.Natl.Acad.Sci.USA 90: 3143-3141.

1 68 1 3432 DNA Cucumber green mottle mosaic virus DNA sequence encoding 129 kD replicase of CGMMV 1 atggcaaaca ttaatgaaca aatcaacaat caacgtgatg ctgctgctag cgggagaaat 60 aatctcgtta gtcagctagc atcaaagagg gtgtatgacg aggccgttcg ctcgttagat 120 catcaagata gacgcccaaa aatgaacttt tctcgtgtgg tcagtacaga gcacaccagg 180 cttgtcaccg atgcgtatcc ggagttttcg attagtttca ccgctaccaa gaattcagtt 240 cattcccttg cgggaggttt gaggcttctt gaattggaat acatgatgat gcaggtgcct 300 tatggttcac cttgctttga tattggcggt aattacacgc agcatttatt taaaggtaga 360 tcatatgtgc attgctgcaa tccgtgcctg gatcttaagg atgttgcgag gaatgtgatg 420 tacaacgaca tgatcacaca acatgtacag aggcacaaag gatctggtgg gtgtagacct 480 cttccgactt tccagataga tgctttcagg aggtatgaag attcgcccgt cgcagtcacc 540 tgtccagacg tttttcaaga atgctcctat gattttggga gtggtaggga taatcatgcg 600 gtttcattac attcgattta tgatatccct tattcttcga ttgggccagc tcttcatagg 660 aaaaacgtca gggtctgtta cgcagccttt catttctcgg aggcgttgct cctaggttcg 720 cccgtgggta atttaaatag tataggggct caatttaggg ttgatggtga cgatgtgcat 780 tttcttttta gtgaggagtc aactttgcat tacactcata gtttggagaa tattaagttg 840 attgtaatgc gtacttattt ccctgctgat gataggttcg tgtatattaa ggagtttatg 900 gttaagcgtg tagacacttt tttttttagg ttagttaggg cagacacaca tatgctccat 960 aaatctgtag ggcactattc gaagtcgaaa tctgagtatt ttgcgttgaa cacccctccg 1020 attttccaag ataaggccac gttttctgtg tggtttcccg aagcgaagcg gaaggtgttg 1080 atacctaagt ttgaactctc gagatttctt tctggaaatg tgaaagtctc taggatgctt 1140 gtcgatgctg attttgtcca taccattatt aatcacatta gcacgtacga taacaaggcc 1200 ttagtgtgga agaatgtcca gtcttttgta gaatctatac gctctagggt aattgtaaac 1260 ggagtttccg taaaatctga atggaatgta ccggtcgatc agcttactga tatctcattc 1320 tcgatattcc ttctcgtgaa ggttagaaag gtgcagattg agttaatgtc tgataaggtt 1380 gtgatcgagg cgaggggttt gcttcggagg ttcgctgata gtctcaaatc cgccgtagaa 1440 ggactaggtg attgcgtcta tgatgctcta gttcaaaccg gttggtttga cacctctagc 1500 gacgaactga aagtattact acctgaaccg tttatgacct tttcagatta tctcgaaggg 1560 atgtacgagg cagatgcaaa aattgagaga gagagtgtct ctgagctgct tgcttccgga 1620 gatgatctgt tcaagaagat tgacgaaata aggaataatt acagcggagt tgaatttgat 1680 gtggagaaat ttcaagaatt ctgtaaagaa ctgaatgtta atcctatgct aatcggtcat 1740 gtgatcgaag ctattttttc acagaaggca ggggtaacag tcacgggcct aggcacgctc 1800 tctcctgaga tgggtgcttc cgttgcgtta tccaataatt ctgtagatac atgtgatgat 1860 atggacgtaa ctgaggatat ggaggaaata gtgttgatag cagacaagaa tcactcttat 1920 atttctccag aaatgtcgag atgggctagt atgaaatacg gcaataataa cggggcctta 1980 gttgagtaca aggtcggaac ctcgatgact ttacctgcca cctgggcaga aaagggtaag 2040 gctgttttac cgttgtcggg aatctgtgta agaaagcccc aattttcaaa gccactcgat 2100 gaggaggacg acttgaggtt atcaaacatg aatttcttta aggtgagtga tctgaagttg 2160 aagaagacta tcactccagt tgtttatact gggaccattc gagagaggca gatgaagaat 2220 tatatcgatt atctatcggc ttctctgggt tctacgcttg gtaatcttga gagaattgtt 2280 aggagtgact ggaatggtac cgaggagagc atgcaaactt ttggattgta cgattgcgag 2340 aagtgcaagt ggttactgtt gccatcggag aagaaacacg cctgggctgt agtcctggcg 2400 agtgatgata ccactcgtat aatctttctg tcgtatgacg aatccggttc tcctataatt 2460 gacaagaaaa attggaagcg gttcgctgtc tgttctgata ccaaagttta tagtgtaatt 2520 cgtagtttag aagtcttaaa taaggaggcc acagtcgatc ctggggtgta tataacttta 2580 gtcgatgggg ttccgggctg tggaaaaacc gctgaaatta tagcgagggt caattggaaa 2640 actgaccttg tgttgactcc cggaagggaa gcggctgcta tgatcaggcg aagagcctgt 2700 gccctacaca agtcacctgt agctactagt gataacgtta ggacttttga ttctttcgta 2760 atgaataaga aggtttttaa atttgacgcc gtctacgtag atgaaggtct tatggtccac 2820 acggggttgc tcaactttgc gttgaagatt tcgggttgta aaaaggcctt tgtcttcggt 2880 gatgctaagc aaattccgtt tattaataga gttatgaatt ttgattatcc taaggaatta 2940 agaactttga tagttgataa tgtagagcgt aggtatatta cccataggtg tcctagagat 3000 gtcactagtt ttcttaatac tatttataaa gctgcggttt ctaccactag tccggttgta 3060 cattccgtga aggcaataaa ggtttctggg gctggtattc tgaggcccga gttgacgaag 3120 atcaaaggga agatcataac gtttactcag tctgataaac aatccttgat caagagtggg 3180 tacaatgatg tgaatactgt gcatgagatt cagggggaga cctttgagga gacggcggtt 3240 gtgcgtgcaa caccgactcc aataggtctg attgcccgag attcaccaca cgtgttagtg 3300 gctttaacgc ggcacaccaa ggcaatggtg tattataccg ttgtgttcga tgccgtaaca 3360 agcataatag cggatgtgga aaaggtcgat cagtcgattt tgactatgtt tgctactact 3420 gtgcctacca aa 3432 2 1144 PRT Cucumber green mottle mosaic virus 129 kD replicase of CGMMV 2 Met Ala Asn Ile Asn Glu Gln Ile Asn Asn Gln Arg Asp Ala Ala Ala 1 5 10 15 Ser Gly Arg Asn Asn Leu Val Ser Gln Leu Ala Ser Lys Arg Val Tyr 20 25 30 Asp Glu Ala Val Arg Ser Leu Asp His Gln Asp Arg Arg Pro Lys Met 35 40 45 Asn Phe Ser Arg Val Val Ser Thr Glu His Thr Arg Leu Val Thr Asp 50 55 60 Ala Tyr Pro Glu Phe Ser Ile Ser Phe Thr Ala Thr Lys Asn Ser Val 65 70 75 80 His Ser Leu Ala Gly Gly Leu Arg Leu Leu Glu Leu Glu Tyr Met Met 85 90 95 Met Gln Val Pro Tyr Gly Ser Pro Cys Phe Asp Ile Gly Gly Asn Tyr 100 105 110 Thr Gln His Leu Phe Lys Gly Arg Ser Tyr Val His Cys Cys Asn Pro 115 120 125 Cys Leu Asp Leu Lys Asp Val Ala Arg Asn Val Met Tyr Asn Asp Met 130 135 140 Ile Thr Gln His Val Gln Arg His Lys Gly Ser Gly Gly Cys Arg Pro 145 150 155 160 Leu Pro Thr Phe Gln Ile Asp Ala Phe Arg Arg Tyr Glu Asp Ser Pro 165 170 175 Val Ala Val Thr Cys Pro Asp Val Phe Gln Glu Cys Ser Tyr Asp Phe 180 185 190 Gly Ser Gly Arg Asp Asn His Ala Val Ser Leu His Ser Ile Tyr Asp 195 200 205 Ile Pro Tyr Ser Ser Ile Gly Pro Ala Leu His Arg Lys Asn Val Arg 210 215 220 Val Cys Tyr Ala Ala Phe His Phe Ser Glu Ala Leu Leu Leu Gly Ser 225 230 235 240 Pro Val Gly Asn Leu Asn Ser Ile Gly Ala Gln Phe Arg Val Asp Gly 245 250 255 Asp Asp Val His Phe Leu Phe Ser Glu Glu Ser Thr Leu His Tyr Thr 260 265 270 His Ser Leu Glu Asn Ile Lys Leu Ile Val Met Arg Thr Tyr Phe Pro 275 280 285 Ala Asp Asp Arg Phe Val Tyr Ile Lys Glu Phe Met Val Lys Arg Val 290 295 300 Asp Thr Phe Phe Phe Arg Leu Val Arg Ala Asp Thr His Met Leu His 305 310 315 320 Lys Ser Val Gly His Tyr Ser Lys Ser Lys Ser Glu Tyr Phe Ala Leu 325 330 335 Asn Thr Pro Pro Ile Phe Gln Asp Lys Ala Thr Phe Ser Val Trp Phe 340 345 350 Pro Glu Ala Lys Arg Lys Val Leu Ile Pro Lys Phe Glu Leu Ser Arg 355 360 365 Phe Leu Ser Gly Asn Val Lys Val Ser Arg Met Leu Val Asp Ala Asp 370 375 380 Phe Val His Thr Ile Ile Asn His Ile Ser Thr Tyr Asp Asn Lys Ala 385 390 395 400 Leu Val Trp Lys Asn Val Gln Ser Phe Val Glu Ser Ile Arg Ser Arg 405 410 415 Val Ile Val Asn Gly Val Ser Val Lys Ser Glu Trp Asn Val Pro Val 420 425 430 Asp Gln Leu Thr Asp Ile Ser Phe Ser Ile Phe Leu Leu Val Lys Val 435 440 445 Arg Lys Val Gln Ile Glu Leu Met Ser Asp Lys Val Val Ile Glu Ala 450 455 460 Arg Gly Leu Leu Arg Arg Phe Ala Asp Ser Leu Lys Ser Ala Val Glu 465 470 475 480 Gly Leu Gly Asp Cys Val Tyr Asp Ala Leu Val Gln Thr Gly Trp Phe 485 490 495 Asp Thr Ser Ser Asp Glu Leu Lys Val Leu Leu Pro Glu Pro Phe Met 500 505 510 Thr Phe Ser Asp Tyr Leu Glu Gly Met Tyr Glu Ala Asp Ala Lys Ile 515 520 525 Glu Arg Glu Ser Val Ser Glu Leu Leu Ala Ser Gly Asp Asp Leu Phe 530 535 540 Lys Lys Ile Asp Glu Ile Arg Asn Asn Tyr Ser Gly Val Glu Phe Asp 545 550 555 560 Val Glu Lys Phe Gln Glu Phe Cys Lys Glu Leu Asn Val Asn Pro Met 565 570 575 Leu Ile Gly His Val Ile Glu Ala Ile Phe Ser Gln Lys Ala Gly Val 580 585 590 Thr Val Thr Gly Leu Gly Thr Leu Ser Pro Glu Met Gly Ala Ser Val 595 600 605 Ala Leu Ser Asn Asn Ser Val Asp Thr Cys Asp Asp Met Asp Val Thr 610 615 620 Glu Asp Met Glu Glu Ile Val Leu Ile Ala Asp Lys Asn His Ser Tyr 625 630 635 640 Ile Ser Pro Glu Met Ser Arg Trp Ala Ser Met Lys Tyr Gly Asn Asn 645 650 655 Asn Gly Ala Leu Val Glu Tyr Lys Val Gly Thr Ser Met Thr Leu Pro 660 665 670 Ala Thr Trp Ala Glu Lys Gly Lys Ala Val Leu Pro Leu Ser Gly Ile 675 680 685 Cys Val Arg Lys Pro Gln Phe Ser Lys Pro Leu Asp Glu Glu Asp Asp 690 695 700 Leu Arg Leu Ser Asn Met Asn Phe Phe Lys Val Ser Asp Leu Lys Leu 705 710 715 720 Lys Lys Thr Ile Thr Pro Val Val Tyr Thr Gly Thr Ile Arg Glu Arg 725 730 735 Gln Met Lys Asn Tyr Ile Asp Tyr Leu Ser Ala Ser Leu Gly Ser Thr 740 745 750 Leu Gly Asn Leu Glu Arg Ile Val Arg Ser Asp Trp Asn Gly Thr Glu 755 760 765 Glu Ser Met Gln Thr Phe Gly Leu Tyr Asp Cys Glu Lys Cys Lys Trp 770 775 780 Leu Leu Leu Pro Ser Glu Lys Lys His Ala Trp Ala Val Val Leu Ala 785 790 795 800 Ser Asp Asp Thr Thr Arg Ile Ile Phe Leu Ser Tyr Asp Glu Ser Gly 805 810 815 Ser Pro Ile Ile Asp Lys Lys Asn Trp Lys Arg Phe Ala Val Cys Ser 820 825 830 Asp Thr Lys Val Tyr Ser Val Ile Arg Ser Leu Glu Val Leu Asn Lys 835 840 845 Glu Ala Thr Val Asp Pro Gly Val Tyr Ile Thr Leu Val Asp Gly Val 850 855 860 Pro Gly Cys Gly Lys Thr Ala Glu Ile Ile Ala Arg Val Asn Trp Lys 865 870 875 880 Thr Asp Leu Val Leu Thr Pro Gly Arg Glu Ala Ala Ala Met Ile Arg 885 890 895 Arg Arg Ala Cys Ala Leu His Lys Ser Pro Val Ala Thr Ser Asp Asn 900 905 910 Val Arg Thr Phe Asp Ser Phe Val Met Asn Lys Lys Val Phe Lys Phe 915 920 925 Asp Ala Val Tyr Val Asp Glu Gly Leu Met Val His Thr Gly Leu Leu 930 935 940 Asn Phe Ala Leu Lys Ile Ser Gly Cys Lys Lys Ala Phe Val Phe Gly 945 950 955 960 Asp Ala Lys Gln Ile Pro Phe Ile Asn Arg Val Met Asn Phe Asp Tyr 965 970 975 Pro Lys Glu Leu Arg Thr Leu Ile Val Asp Asn Val Glu Arg Arg Tyr 980 985 990 Ile Thr His Arg Cys Pro Arg Asp Val Thr Ser Phe Leu Asn Thr Ile 995 1000 1005 Tyr Lys Ala Ala Val Ser Thr Thr Ser Pro Val Val His Ser Val Lys 1010 1015 1020 Ala Ile Lys Val Ser Gly Ala Gly Ile Leu Arg Pro Glu Leu Thr Lys 1025 1030 1035 1040 Ile Lys Gly Lys Ile Ile Thr Phe Thr Gln Ser Asp Lys Gln Ser Leu 1045 1050 1055 Ile Lys Ser Gly Tyr Asn Asp Val Asn Thr Val His Glu Ile Gln Gly 1060 1065 1070 Glu Thr Phe Glu Glu Thr Ala Val Val Arg Ala Thr Pro Thr Pro Ile 1075 1080 1085 Gly Leu Ile Ala Arg Asp Ser Pro His Val Leu Val Ala Leu Thr Arg 1090 1095 1100 His Thr Lys Ala Met Val Tyr Tyr Thr Val Val Phe Asp Ala Val Thr 1105 1110 1115 1120 Ser Ile Ile Ala Asp Val Glu Lys Val Asp Gln Ser Ile Leu Thr Met 1125 1130 1135 Phe Ala Thr Thr Val Pro Thr Lys 1140 3 1503 DNA Cucumber green mottle mosaic virus DNA sequence encoding 57 kD protein of CGMMV 3 atggagaatt cgctgtatgt ccaccgcaat atcttcctcc ctgttactaa gacagggttt 60 tatacggata tgcaggagtt ctatgacagg tgtcttccag ggaattcttt tgttctgaac 120 gatttcgatg ccgtcaccat gcggttgagg gataatgaat tcaatttgca accttgtaga 180 ttaactttaa gtaatttaga tccggtgccg gctttgatta agagtgaggc aaaagatttt 240 ctggttcccg tattgcgaac ggcttgcgaa aggccgcgta ttccgggtct tctcgaaaat 300 cttgttgcta tgataaagag gaatatgaat actcctgatt tggctgggac cgtggatata 360 actaatatgt ctatttctat agtagataat ttcttttctt cctttgtcag ggacgaggtt 420 ctacttgatc atttagattg cgttagagct agttctattc agagtttttc cgattggttt 480 tcttgtcagc caacctcggc ggttggccag ttagctaatt ttaacttcat agatttacct 540 gcctttgata cgtatatgca tatgattaaa aggcagccta agagtcggtt agatacttcg 600 attcagtccg aatatccggc cttacaaact attgtatatc atccgaaggt ggtaaacgca 660 gttttcgggc cggtttttaa gtatctgact actaagtttc ttagcatggt agataattct 720 aagtttttct tttatactag gaaaaagcca gaggatctgc aggaattttt ctcggatctt 780 tcttcccatt ctgattatga aattcttgag ctcgatgttt ctaaatatga taagtcgcag 840 tccgatttcc atttctctat cgagatggca atttgggaaa ggctgggact agatgatatt 900 ttagcttgga tgtggtctat gggtcataag agaactatac tgcaagattt ccaagctgga 960 ataaagacgc tcatttatta tcaaaggaag tctggcgacg taactacttt cataggtaat 1020 acttttatta ttgcagcgtg tgtagctagt atgttaccgt tagataagtg ttttaaggct 1080 agtttttgtg gtgatgattc gttaatctac cttcctaagg gtttggagta tcctgatatt 1140 caggctactg ccaatttggt ttggaatttt gaggcgaaac ttttccggaa gaagtatggt 1200 tacttctgcg ggaaatatat cattcatcac gccaacggtt gtattgttta ccctgaccct 1260 ttgaagttaa ttagtaaatt aggtagtaag agtcttgtag ggtacgagca tgtcgaggag 1320 tttcgtatat ctctcctcga tgtcgctcac agtttgttta atggtgctta tttccatttg 1380 ctcgacgatg caatccacga gttgtttcct aacgctgggg gttgcagttt tgtaataaat 1440 tgtttgtgta agtacttgag tgataagcgc cttttccgta gtctttatat agatgtctct 1500 aag 1503 4 501 PRT Cucumber green mottle mosaic virus 57 kD protein of CGMMV 4 Met Glu Asn Ser Leu Tyr Val His Arg Asn Ile Phe Leu Pro Val Thr 1 5 10 15 Lys Thr Gly Phe Tyr Thr Asp Met Gln Glu Phe Tyr Asp Arg Cys Leu 20 25 30 Pro Gly Asn Ser Phe Val Leu Asn Asp Phe Asp Ala Val Thr Met Arg 35 40 45 Leu Arg Asp Asn Glu Phe Asn Leu Gln Pro Cys Arg Leu Thr Leu Ser 50 55 60 Asn Leu Asp Pro Val Pro Ala Leu Ile Lys Ser Glu Ala Lys Asp Phe 65 70 75 80 Leu Val Pro Val Leu Arg Thr Ala Cys Glu Arg Pro Arg Ile Pro Gly 85 90 95 Leu Leu Glu Asn Leu Val Ala Met Ile Lys Arg Asn Met Asn Thr Pro 100 105 110 Asp Leu Ala Gly Thr Val Asp Ile Thr Asn Met Ser Ile Ser Ile Val 115 120 125 Asp Asn Phe Phe Ser Ser Phe Val Arg Asp Glu Val Leu Leu Asp His 130 135 140 Leu Asp Cys Val Arg Ala Ser Ser Ile Gln Ser Phe Ser Asp Trp Phe 145 150 155 160 Ser Cys Gln Pro Thr Ser Ala Val Gly Gln Leu Ala Asn Phe Asn Phe 165 170 175 Ile Asp Leu Pro Ala Phe Asp Thr Tyr Met His Met Ile Lys Arg Gln 180 185 190 Pro Lys Ser Arg Leu Asp Thr Ser Ile Gln Ser Glu Tyr Pro Ala Leu 195 200 205 Gln Thr Ile Val Tyr His Pro Lys Val Val Asn Ala Val Phe Gly Pro 210 215 220 Val Phe Lys Tyr Leu Thr Thr Lys Phe Leu Ser Met Val Asp Asn Ser 225 230 235 240 Lys Phe Phe Phe Tyr Thr Arg Lys Lys Pro Glu Asp Leu Gln Glu Phe 245 250 255 Phe Ser Asp Leu Ser Ser His Ser Asp Tyr Glu Ile Leu Glu Leu Asp 260 265 270 Val Ser Lys Tyr Asp Lys Ser Gln Ser Asp Phe His Phe Ser Ile Glu 275 280 285 Met Ala Ile Trp Glu Arg Leu Gly Leu Asp Asp Ile Leu Ala Trp Met 290 295 300 Trp Ser Met Gly His Lys Arg Thr Ile Leu Gln Asp Phe Gln Ala Gly 305 310 315 320 Ile Lys Thr Leu Ile Tyr Tyr Gln Arg Lys Ser Gly Asp Val Thr Thr 325 330 335 Phe Ile Gly Asn Thr Phe Ile Ile Ala Ala Cys Val Ala Ser Met Leu 340 345 350 Pro Leu Asp Lys Cys Phe Lys Ala Ser Phe Cys Gly Asp Asp Ser Leu 355 360 365 Ile Tyr Leu Pro Lys Gly Leu Glu Tyr Pro Asp Ile Gln Ala Thr Ala 370 375 380 Asn Leu Val Trp Asn Phe Glu Ala Lys Leu Phe Arg Lys Lys Tyr Gly 385 390 395 400 Tyr Phe Cys Gly Lys Tyr Ile Ile His His Ala Asn Gly Cys Ile Val 405 410 415 Tyr Pro Asp Pro Leu Lys Leu Ile Ser Lys Leu Gly Ser Lys Ser Leu 420 425 430 Val Gly Tyr Glu His Val Glu Glu Phe Arg Ile Ser Leu Leu Asp Val 435 440 445 Ala His Ser Leu Phe Asn Gly Ala Tyr Phe His Leu Leu Asp Asp Ala 450 455 460 Ile His Glu Leu Phe Pro Asn Ala Gly Gly Cys Ser Phe Val Ile Asn 465 470 475 480 Cys Leu Cys Lys Tyr Leu Ser Asp Lys Arg Leu Phe Arg Ser Leu Tyr 485 490 495 Ile Asp Val Ser Lys 500 5 4935 DNA Cucumber green mottle mosaic virus DNA sequence encoding 186 kDa protein of CGMMV 5 atggcaaaca ttaatgaaca aatcaacaat caacgtgatg ctgctgctag cgggagaaat 60 aatctcgtta gtcagctagc atcaaagagg gtgtatgacg aggccgttcg ctcgttagat 120 catcaagata gacgcccaaa aatgaacttt tctcgtgtgg tcagtacaga gcacaccagg 180 cttgtcaccg atgcgtatcc ggagttttcg attagtttca ccgctaccaa gaattcagtt 240 cattcccttg cgggaggttt gaggcttctt gaattggaat acatgatgat gcaggtgcct 300 tatggttcac cttgctttga tattggcggt aattacacgc agcatttatt taaaggtaga 360 tcatatgtgc attgctgcaa tccgtgcctg gatcttaagg atgttgcgag gaatgtgatg 420 tacaacgaca tgatcacaca acatgtacag aggcacaaag gatctggtgg gtgtagacct 480 cttccgactt tccagataga tgctttcagg aggtatgaag attcgcccgt cgcagtcacc 540 tgtccagacg tttttcaaga atgctcctat gattttggga gtggtaggga taatcatgcg 600 gtttcattac attcgattta tgatatccct tattcttcga ttgggccagc tcttcatagg 660 aaaaacgtca gggtctgtta cgcagccttt catttctcgg aggcgttgct cctaggttcg 720 cccgtgggta atttaaatag tataggggct caatttaggg ttgatggtga cgatgtgcat 780 tttcttttta gtgaggagtc aactttgcat tacactcata gtttggagaa tattaagttg 840 attgtaatgc gtacttattt ccctgctgat gataggttcg tgtatattaa ggagtttatg 900 gttaagcgtg tagacacttt tttttttagg ttagttaggg cagacacaca tatgctccat 960 aaatctgtag ggcactattc gaagtcgaaa tctgagtatt ttgcgttgaa cacccctccg 1020 attttccaag ataaggccac gttttctgtg tggtttcccg aagcgaagcg gaaggtgttg 1080 atacctaagt ttgaactctc gagatttctt tctggaaatg tgaaagtctc taggatgctt 1140 gtcgatgctg attttgtcca taccattatt aatcacatta gcacgtacga taacaaggcc 1200 ttagtgtgga agaatgtcca gtcttttgta gaatctatac gctctagggt aattgtaaac 1260 ggagtttccg taaaatctga atggaatgta ccggtcgatc agcttactga tatctcattc 1320 tcgatattcc ttctcgtgaa ggttagaaag gtgcagattg agttaatgtc tgataaggtt 1380 gtgatcgagg cgaggggttt gcttcggagg ttcgctgata gtctcaaatc cgccgtagaa 1440 ggactaggtg attgcgtcta tgatgctcta gttcaaaccg gttggtttga cacctctagc 1500 gacgaactga aagtattact acctgaaccg tttatgacct tttcagatta tctcgaaggg 1560 atgtacgagg cagatgcaaa aattgagaga gagagtgtct ctgagctgct tgcttccgga 1620 gatgatctgt tcaagaagat tgacgaaata aggaataatt acagcggagt tgaatttgat 1680 gtggagaaat ttcaagaatt ctgtaaagaa ctgaatgtta atcctatgct aatcggtcat 1740 gtgatcgaag ctattttttc acagaaggca ggggtaacag tcacgggcct aggcacgctc 1800 tctcctgaga tgggtgcttc cgttgcgtta tccaataatt ctgtagatac atgtgatgat 1860 atggacgtaa ctgaggatat ggaggaaata gtgttgatag cagacaagaa tcactcttat 1920 atttctccag aaatgtcgag atgggctagt atgaaatacg gcaataataa cggggcctta 1980 gttgagtaca aggtcggaac ctcgatgact ttacctgcca cctgggcaga aaagggtaag 2040 gctgttttac cgttgtcggg aatctgtgta agaaagcccc aattttcaaa gccactcgat 2100 gaggaggacg acttgaggtt atcaaacatg aatttcttta aggtgagtga tctgaagttg 2160 aagaagacta tcactccagt tgtttatact gggaccattc gagagaggca gatgaagaat 2220 tatatcgatt atctatcggc ttctctgggt tctacgcttg gtaatcttga gagaattgtt 2280 aggagtgact ggaatggtac cgaggagagc atgcaaactt ttggattgta cgattgcgag 2340 aagtgcaagt ggttactgtt gccatcggag aagaaacacg cctgggctgt agtcctggcg 2400 agtgatgata ccactcgtat aatctttctg tcgtatgacg aatccggttc tcctataatt 2460 gacaagaaaa attggaagcg gttcgctgtc tgttctgata ccaaagttta tagtgtaatt 2520 cgtagtttag aagtcttaaa taaggaggcc acagtcgatc ctggggtgta tataacttta 2580 gtcgatgggg ttccgggctg tggaaaaacc gctgaaatta tagcgagggt caattggaaa 2640 actgaccttg tgttgactcc cggaagggaa gcggctgcta tgatcaggcg aagagcctgt 2700 gccctacaca agtcacctgt agctactagt gataacgtta ggacttttga ttctttcgta 2760 atgaataaga aggtttttaa atttgacgcc gtctacgtag atgaaggtct tatggtccac 2820 acggggttgc tcaactttgc gttgaagatt tcgggttgta aaaaggcctt tgtcttcggt 2880 gatgctaagc aaattccgtt tattaataga gttatgaatt ttgattatcc taaggaatta 2940 agaactttga tagttgataa tgtagagcgt aggtatatta cccataggtg tcctagagat 3000 gtcactagtt ttcttaatac tatttataaa gctgcggttt ctaccactag tccggttgta 3060 cattccgtga aggcaataaa ggtttctggg gctggtattc tgaggcccga gttgacgaag 3120 atcaaaggga agatcataac gtttactcag tctgataaac aatccttgat caagagtggg 3180 tacaatgatg tgaatactgt gcatgagatt cagggggaga cctttgagga gacggcggtt 3240 gtgcgtgcaa caccgactcc aataggtctg attgcccgag attcaccaca cgtgttagtg 3300 gctttaacgc ggcacaccaa ggcaatggtg tattataccg ttgtgttcga tgccgtaaca 3360 agcataatag cggatgtgga aaaggtcgat cagtcgattt tgactatgtt tgctactact 3420 gtgcctacca aaatggagaa ttcgctgtat gtccaccgca atatcttcct ccctgttact 3480 aagacagggt tttatacgga tatgcaggag ttctatgaca ggtgtcttcc agggaattct 3540 tttgttctga acgatttcga tgccgtcacc atgcggttga gggataatga attcaatttg 3600 caaccttgta gattaacttt aagtaattta gatccggtgc cggctttgat taagagtgag 3660 gcaaaagatt ttctggttcc cgtattgcga acggcttgcg aaaggccgcg tattccgggt 3720 cttctcgaaa atcttgttgc tatgataaag aggaatatga atactcctga tttggctggg 3780 accgtggata taactaatat gtctatttct atagtagata atttcttttc ttcctttgtc 3840 agggacgagg ttctacttga tcatttagat tgcgttagag ctagttctat tcagagtttt 3900 tccgattggt tttcttgtca gccaacctcg gcggttggcc agttagctaa ttttaacttc 3960 atagatttac ctgcctttga tacgtatatg catatgatta aaaggcagcc taagagtcgg 4020 ttagatactt cgattcagtc cgaatatccg gccttacaaa ctattgtata tcatccgaag 4080 gtggtaaacg cagttttcgg gccggttttt aagtatctga ctactaagtt tcttagcatg 4140 gtagataatt ctaagttttt cttttatact aggaaaaagc cagaggatct gcaggaattt 4200 ttctcggatc tttcttccca ttctgattat gaaattcttg agctcgatgt ttctaaatat 4260 gataagtcgc agtccgattt ccatttctct atcgagatgg caatttggga aaggctggga 4320 ctagatgata ttttagcttg gatgtggtct atgggtcata agagaactat actgcaagat 4380 ttccaagctg gaataaagac gctcatttat tatcaaagga agtctggcga cgtaactact 4440 ttcataggta atacttttat tattgcagcg tgtgtagcta gtatgttacc gttagataag 4500 tgttttaagg ctagtttttg tggtgatgat tcgttaatct accttcctaa gggtttggag 4560 tatcctgata ttcaggctac tgccaatttg gtttggaatt ttgaggcgaa acttttccgg 4620 aagaagtatg gttacttctg cgggaaatat atcattcatc acgccaacgg ttgtattgtt 4680 taccctgacc ctttgaagtt aattagtaaa ttaggtagta agagtcttgt agggtacgag 4740 catgtcgagg agtttcgtat atctctcctc gatgtcgctc acagtttgtt taatggtgct 4800 tatttccatt tgctcgacga tgcaatccac gagttgtttc ctaacgctgg gggttgcagt 4860 tttgtaataa attgtttgtg taagtacttg agtgataagc gccttttccg tagtctttat 4920 atagatgtct ctaag 4935 6 1645 PRT Cucumber green mottle mosaic virus 186 kD protein of CGMMV 6 Met Ala Asn Ile Asn Glu Gln Ile Asn Asn Gln Arg Asp Ala Ala Ala 1 5 10 15 Ser Gly Arg Asn Asn Leu Val Ser Gln Leu Ala Ser Lys Arg Val Tyr 20 25 30 Asp Glu Ala Val Arg Ser Leu Asp His Gln Asp Arg Arg Pro Lys Met 35 40 45 Asn Phe Ser Arg Val Val Ser Thr Glu His Thr Arg Leu Val Thr Asp 50 55 60 Ala Tyr Pro Glu Phe Ser Ile Ser Phe Thr Ala Thr Lys Asn Ser Val 65 70 75 80 His Ser Leu Ala Gly Gly Leu Arg Leu Leu Glu Leu Glu Tyr Met Met 85 90 95 Met Gln Val Pro Tyr Gly Ser Pro Cys Phe Asp Ile Gly Gly Asn Tyr 100 105 110 Thr Gln His Leu Phe Lys Gly Arg Ser Tyr Val His Cys Cys Asn Pro 115 120 125 Cys Leu Asp Leu Lys Asp Val Ala Arg Asn Val Met Tyr Asn Asp Met 130 135 140 Ile Thr Gln His Val Gln Arg His Lys Gly Ser Gly Gly Cys Arg Pro 145 150 155 160 Leu Pro Thr Phe Gln Ile Asp Ala Phe Arg Arg Tyr Glu Asp Ser Pro 165 170 175 Val Ala Val Thr Cys Pro Asp Val Phe Gln Glu Cys Ser Tyr Asp Phe 180 185 190 Gly Ser Gly Arg Asp Asn His Ala Val Ser Leu His Ser Ile Tyr Asp 195 200 205 Ile Pro Tyr Ser Ser Ile Gly Pro Ala Leu His Arg Lys Asn Val Arg 210 215 220 Val Cys Tyr Ala Ala Phe His Phe Ser Glu Ala Leu Leu Leu Gly Ser 225 230 235 240 Pro Val Gly Asn Leu Asn Ser Ile Gly Ala Gln Phe Arg Val Asp Gly 245 250 255 Asp Asp Val His Phe Leu Phe Ser Glu Glu Ser Thr Leu His Tyr Thr 260 265 270 His Ser Leu Glu Asn Ile Lys Leu Ile Val Met Arg Thr Tyr Phe Pro 275 280 285 Ala Asp Asp Arg Phe Val Tyr Ile Lys Glu Phe Met Val Lys Arg Val 290 295 300 Asp Thr Phe Phe Phe Arg Leu Val Arg Ala Asp Thr His Met Leu His 305 310 315 320 Lys Ser Val Gly His Tyr Ser Lys Ser Lys Ser Glu Tyr Phe Ala Leu 325 330 335 Asn Thr Pro Pro Ile Phe Gln Asp Lys Ala Thr Phe Ser Val Trp Phe 340 345 350 Pro Glu Ala Lys Arg Lys Val Leu Ile Pro Lys Phe Glu Leu Ser Arg 355 360 365 Phe Leu Ser Gly Asn Val Lys Val Ser Arg Met Leu Val Asp Ala Asp 370 375 380 Phe Val His Thr Ile Ile Asn His Ile Ser Thr Tyr Asp Asn Lys Ala 385 390 395 400 Leu Val Trp Lys Asn Val Gln Ser Phe Val Glu Ser Ile Arg Ser Arg 405 410 415 Val Ile Val Asn Gly Val Ser Val Lys Ser Glu Trp Asn Val Pro Val 420 425 430 Asp Gln Leu Thr Asp Ile Ser Phe Ser Ile Phe Leu Leu Val Lys Val 435 440 445 Arg Lys Val Gln Ile Glu Leu Met Ser Asp Lys Val Val Ile Glu Ala 450 455 460 Arg Gly Leu Leu Arg Arg Phe Ala Asp Ser Leu Lys Ser Ala Val Glu 465 470 475 480 Gly Leu Gly Asp Cys Val Tyr Asp Ala Leu Val Gln Thr Gly Trp Phe 485 490 495 Asp Thr Ser Ser Asp Glu Leu Lys Val Leu Leu Pro Glu Pro Phe Met 500 505 510 Thr Phe Ser Asp Tyr Leu Glu Gly Met Tyr Glu Ala Asp Ala Lys Ile 515 520 525 Glu Arg Glu Ser Val Ser Glu Leu Leu Ala Ser Gly Asp Asp Leu Phe 530 535 540 Lys Lys Ile Asp Glu Ile Arg Asn Asn Tyr Ser Gly Val Glu Phe Asp 545 550 555 560 Val Glu Lys Phe Gln Glu Phe Cys Lys Glu Leu Asn Val Asn Pro Met 565 570 575 Leu Ile Gly His Val Ile Glu Ala Ile Phe Ser Gln Lys Ala Gly Val 580 585 590 Thr Val Thr Gly Leu Gly Thr Leu Ser Pro Glu Met Gly Ala Ser Val 595 600 605 Ala Leu Ser Asn Asn Ser Val Asp Thr Cys Asp Asp Met Asp Val Thr 610 615 620 Glu Asp Met Glu Glu Ile Val Leu Ile Ala Asp Lys Asn His Ser Tyr 625 630 635 640 Ile Ser Pro Glu Met Ser Arg Trp Ala Ser Met Lys Tyr Gly Asn Asn 645 650 655 Asn Gly Ala Leu Val Glu Tyr Lys Val Gly Thr Ser Met Thr Leu Pro 660 665 670 Ala Thr Trp Ala Glu Lys Gly Lys Ala Val Leu Pro Leu Ser Gly Ile 675 680 685 Cys Val Arg Lys Pro Gln Phe Ser Lys Pro Leu Asp Glu Glu Asp Asp 690 695 700 Leu Arg Leu Ser Asn Met Asn Phe Phe Lys Val Ser Asp Leu Lys Leu 705 710 715 720 Lys Lys Thr Ile Thr Pro Val Val Tyr Thr Gly Thr Ile Arg Glu Arg 725 730 735 Gln Met Lys Asn Tyr Ile Asp Tyr Leu Ser Ala Ser Leu Gly Ser Thr 740 745 750 Leu Gly Asn Leu Glu Arg Ile Val Arg Ser Asp Trp Asn Gly Thr Glu 755 760 765 Glu Ser Met Gln Thr Phe Gly Leu Tyr Asp Cys Glu Lys Cys Lys Trp 770 775 780 Leu Leu Leu Pro Ser Glu Lys Lys His Ala Trp Ala Val Val Leu Ala 785 790 795 800 Ser Asp Asp Thr Thr Arg Ile Ile Phe Leu Ser Tyr Asp Glu Ser Gly 805 810 815 Ser Pro Ile Ile Asp Lys Lys Asn Trp Lys Arg Phe Ala Val Cys Ser 820 825 830 Asp Thr Lys Val Tyr Ser Val Ile Arg Ser Leu Glu Val Leu Asn Lys 835 840 845 Glu Ala Thr Val Asp Pro Gly Val Tyr Ile Thr Leu Val Asp Gly Val 850 855 860 Pro Gly Cys Gly Lys Thr Ala Glu Ile Ile Ala Arg Val Asn Trp Lys 865 870 875 880 Thr Asp Leu Val Leu Thr Pro Gly Arg Glu Ala Ala Ala Met Ile Arg 885 890 895 Arg Arg Ala Cys Ala Leu His Lys Ser Pro Val Ala Thr Ser Asp Asn 900 905 910 Val Arg Thr Phe Asp Ser Phe Val Met Asn Lys Lys Val Phe Lys Phe 915 920 925 Asp Ala Val Tyr Val Asp Glu Gly Leu Met Val His Thr Gly Leu Leu 930 935 940 Asn Phe Ala Leu Lys Ile Ser Gly Cys Lys Lys Ala Phe Val Phe Gly 945 950 955 960 Asp Ala Lys Gln Ile Pro Phe Ile Asn Arg Val Met Asn Phe Asp Tyr 965 970 975 Pro Lys Glu Leu Arg Thr Leu Ile Val Asp Asn Val Glu Arg Arg Tyr 980 985 990 Ile Thr His Arg Cys Pro Arg Asp Val Thr Ser Phe Leu Asn Thr Ile 995 1000 1005 Tyr Lys Ala Ala Val Ser Thr Thr Ser Pro Val Val His Ser Val Lys 1010 1015 1020 Ala Ile Lys Val Ser Gly Ala Gly Ile Leu Arg Pro Glu Leu Thr Lys 1025 1030 1035 1040 Ile Lys Gly Lys Ile Ile Thr Phe Thr Gln Ser Asp Lys Gln Ser Leu 1045 1050 1055 Ile Lys Ser Gly Tyr Asn Asp Val Asn Thr Val His Glu Ile Gln Gly 1060 1065 1070 Glu Thr Phe Glu Glu Thr Ala Val Val Arg Ala Thr Pro Thr Pro Ile 1075 1080 1085 Gly Leu Ile Ala Arg Asp Ser Pro His Val Leu Val Ala Leu Thr Arg 1090 1095 1100 His Thr Lys Ala Met Val Tyr Tyr Thr Val Val Phe Asp Ala Val Thr 1105 1110 1115 1120 Ser Ile Ile Ala Asp Val Glu Lys Val Asp Gln Ser Ile Leu Thr Met 1125 1130 1135 Phe Ala Thr Thr Val Pro Thr Lys Met Glu Asn Ser Leu Tyr Val His 1140 1145 1150 Arg Asn Ile Phe Leu Pro Val Thr Lys Thr Gly Phe Tyr Thr Asp Met 1155 1160 1165 Gln Glu Phe Tyr Asp Arg Cys Leu Pro Gly Asn Ser Phe Val Leu Asn 1170 1175 1180 Asp Phe Asp Ala Val Thr Met Arg Leu Arg Asp Asn Glu Phe Asn Leu 1185 1190 1195 1200 Gln Pro Cys Arg Leu Thr Leu Ser Asn Leu Asp Pro Val Pro Ala Leu 1205 1210 1215 Ile Lys Ser Glu Ala Lys Asp Phe Leu Val Pro Val Leu Arg Thr Ala 1220 1225 1230 Cys Glu Arg Pro Arg Ile Pro Gly Leu Leu Glu Asn Leu Val Ala Met 1235 1240 1245 Ile Lys Arg Asn Met Asn Thr Pro Asp Leu Ala Gly Thr Val Asp Ile 1250 1255 1260 Thr Asn Met Ser Ile Ser Ile Val Asp Asn Phe Phe Ser Ser Phe Val 1265 1270 1275 1280 Arg Asp Glu Val Leu Leu Asp His Leu Asp Cys Val Arg Ala Ser Ser 1285 1290 1295 Ile Gln Ser Phe Ser Asp Trp Phe Ser Cys Gln Pro Thr Ser Ala Val 1300 1305 1310 Gly Gln Leu Ala Asn Phe Asn Phe Ile Asp Leu Pro Ala Phe Asp Thr 1315 1320 1325 Tyr Met His Met Ile Lys Arg Gln Pro Lys Ser Arg Leu Asp Thr Ser 1330 1335 1340 Ile Gln Ser Glu Tyr Pro Ala Leu Gln Thr Ile Val Tyr His Pro Lys 1345 1350 1355 1360 Val Val Asn Ala Val Phe Gly Pro Val Phe Lys Tyr Leu Thr Thr Lys 1365 1370 1375 Phe Leu Ser Met Val Asp Asn Ser Lys Phe Phe Phe Tyr Thr Arg Lys 1380 1385 1390 Lys Pro Glu Asp Leu Gln Glu Phe Phe Ser Asp Leu Ser Ser His Ser 1395 1400 1405 Asp Tyr Glu Ile Leu Glu Leu Asp Val Ser Lys Tyr Asp Lys Ser Gln 1410 1415 1420 Ser Asp Phe His Phe Ser Ile Glu Met Ala Ile Trp Glu Arg Leu Gly 1425 1430 1435 1440 Leu Asp Asp Ile Leu Ala Trp Met Trp Ser Met Gly His Lys Arg Thr 1445 1450 1455 Ile Leu Gln Asp Phe Gln Ala Gly Ile Lys Thr Leu Ile Tyr Tyr Gln 1460 1465 1470 Arg Lys Ser Gly Asp Val Thr Thr Phe Ile Gly Asn Thr Phe Ile Ile 1475 1480 1485 Ala Ala Cys Val Ala Ser Met Leu Pro Leu Asp Lys Cys Phe Lys Ala 1490 1495 1500 Ser Phe Cys Gly Asp Asp Ser Leu Ile Tyr Leu Pro Lys Gly Leu Glu 1505 1510 1515 1520 Tyr Pro Asp Ile Gln Ala Thr Ala Asn Leu Val Trp Asn Phe Glu Ala 1525 1530 1535 Lys Leu Phe Arg Lys Lys Tyr Gly Tyr Phe Cys Gly Lys Tyr Ile Ile 1540 1545 1550 His His Ala Asn Gly Cys Ile Val Tyr Pro Asp Pro Leu Lys Leu Ile 1555 1560 1565 Ser Lys Leu Gly Ser Lys Ser Leu Val Gly Tyr Glu His Val Glu Glu 1570 1575 1580 Phe Arg Ile Ser Leu Leu Asp Val Ala His Ser Leu Phe Asn Gly Ala 1585 1590 1595 1600 Tyr Phe His Leu Leu Asp Asp Ala Ile His Glu Leu Phe Pro Asn Ala 1605 1610 1615 Gly Gly Cys Ser Phe Val Ile Asn Cys Leu Cys Lys Tyr Leu Ser Asp 1620 1625 1630 Lys Arg Leu Phe Arg Ser Leu Tyr Ile Asp Val Ser Lys 1635 1640 1645 7 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 1 7 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtaatggc gagagacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccagttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgctc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttc caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtt gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ccttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gaatcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 8 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 2 8 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtaatggc gagagacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccagttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgctc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttc caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtt gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gaatcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 9 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 3 9 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtaatggc gagagacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggtattc taaacctcca aatcggaggt 480 cgggctctgc ttctgaagag tccagttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgttc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttc caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtc gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gtttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gagtcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaaaggg tttgatgttt atgatagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 10 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 4 10 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctccgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtttagt tgccactact aactctatta ttaaaagggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcag ctgtaatggc gagagacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccggttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgttc ccgttagaac tctacttaat 600 tttctggtgg cgtcgcaagg tactgctttc caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtc gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gagtcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 11 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 5 11 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctccgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtttagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcag ctgtaatggc gagagacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccggttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgttc ccgttagaac tctacttaat 600 tttctggtgg cgtcgcaagg tactgctttc caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtc gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gagtcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 12 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isloate 6 12 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaagga gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtaatggc gagagacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccagttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgttc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttc caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtt gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gaatcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgacagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 13 1138 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 7 13 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtgatggc gagggacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccagttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgttc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttc caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtt gtagatatta attctaggtt cccgaatgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgttgatc ctagcaatcc gacgactgct 840 gagtcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa ctctcgcgtg tgacgttgaa gtttctatgg gcaagccg 1138 14 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 8 14 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggttg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggtattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttatctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtaatggc gagagacccc agttataggt 420 ctaggtcgca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccagttctg tttctttcga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcttatgctc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttc caaatccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtt gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gaatcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcttttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 15 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 9 15 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggctg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggcattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttgtctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtaatggc tagagacccc agttataggt 420 ctaggtcaca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccagttctg tttcttttga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcatatgttc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttt caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtt gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gagtcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcctttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgttttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 16 1139 DNA Cucumber green mottle mosaic virus DNA sequence encoding coat protein of CGMMV isolate 10 16 aattcggctt ctgtaggggt ggtgctactg ttgctttggt tgacacaagg atgcattctg 60 ttgcagaagg aactatatgc aaattttcag ctcccgccac cgtccgcgag ttctctgtta 120 ggttcatccc taactattct gtcgtggctg cggatgccct tcgcgatcct tggtctttat 180 ttgtgaggct ctctaacgta ggcattaagg atggttttca tccattaact ttagaggtcg 240 cctgtctagt tgccactact aactctatta ttaaaaaggg gcttagagct tctgtagttg 300 agtccgttgt ctcttccgat cagtcgattg ttctagattc tttgtctgag aaagttgagc 360 ctttcttcga taaagtccct atttcagcgg ctgtaatggc tagagacccc agttataggt 420 ctaggtcaca gtctgtcgtt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 cggactctgc ttctgaagag tccagttctg tttcttttga agatggctta caatccgatc 540 acgcctagca aacttattgc gtttagtgct tcatatgttc ccgttagaac tttacttaat 600 tttctagtgg cgtcgcaagg tactgctttt caaacccagg caggaagaga ttccttccgt 660 gagtctttgt ctgcgttacc ttcatccgtt gtagatatta attctaggtt cccgagtgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttcttagc 780 tctacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc gacgactgct 840 gagtcgctta acgcagttaa gcgtactgac gatgcgtcta cagccgctag ggctgagata 900 gataatttaa tagaatcaat ctctaagggg tttgatgttt atgatagggc ttcctttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcca aggcttagcc ttgagggtct 1020 tctgacggtg gtgcacacca tagtgcatag tgctttcccg ttcactttaa tcgaacggtt 1080 tgctcattgg tttgcgaaaa cctctcgcgt gtgacgttga agtttctatg ggcaagccg 1139 17 3429 DNA Cucumber green mottle mosaic virus DNA sequence encoding 129 kD replicase of CGMMV strain SH 17 atggcaaaca ttaatgaaca aatcaacaac caacgtgacg ccgcggctag cgggagaaac 60 aatctcgtta gccaattggc gtcaaaaagg gtgtatgacg aggctgttcg ctcgttggat 120 catcaagaca gacgcccgaa aatgaatttt tctcgtgtgg tcagcacaga gcacaccagg 180 cttgtaactg acgcgtatcc ggagttttcg attagcttta ccgccaccaa gaactctgta 240 cactcccttg cgggtggtct gaggcttctt gaattggaat atatgatgat gcaggtgccc 300 tacggctcac cttgttatga catcggcggt aactatacgc agcacttgtt caaaggtaga 360 tcatatgtgc attgctgcaa tccgtgccta gatcttaagg atgttgcgag gaatgtgatg 420 tacaacgata tgattacgca acatgtacag aggcacaagg gatcttgcgg gtgcagacct 480 cttccaactt tccagataga tgcattcagg aggtacgata gttctccctg tgcggtcacc 540 tgttcagacg ttttccaaga gtgttcctat gattttggga gtggtaggga taatcatgca 600 gtctcgttgc attcaatcta cgatatccct tattcttcga tcggacctgc tcttcatagg 660 aagaatgtgc gagtttgtta tgcagccttt catttctcgg aggcattgct tttaggttcg 720 cctgtaggta atttaaatag tattggggct cagtttaggg tcgatggtga tgatgtgcat 780 tttcttttta gtgaagagtc tactttgcat tatactcata gtttagaaaa tatcaagtta 840 atcgtgatgc gtacttactt tcctgctgat gataggtttg tatatattaa ggagttcatg 900 gttaagcgtg tggatacttt tttctttagg ttggtcagag cagatacaca catgcttcat 960 aaatctgtgg ggcactattc gaaatcgaag tctgagtact tcgcgctgaa tacccctccg 1020 atcttccaag ataaagccac gttttctgtg tggtttcctg aagcgaagaa ggtgttgata 1080 cccaagtttg aactttcgag attcctttct gggaatgtga aaatctctag gatgcttgtc 1140 gatgctgatt tcgtccatac cattattaat cacattagca cgtatgataa caaggcctta 1200 gtgtggaaga atgttcagtc ctttgtggaa tccatacgtt caagagtaat tgtaaacgga 1260 gtttccgtga aatctgagtg gaacgtaccg gttgatcagc tcactgatat ctcgttctcg 1320 atattccctc tcgtgaaggt taggaaggta cagatcgagt taatgtctga taaagttgta 1380 atcgaggcga ggggtttgct tcggaggttc gcagacagtc ttaaatctgc cgtagaagga 1440 ctaggtgatt gcgtctatga tgctctagtt caaaccggct ggtttgacac ctctagcgac 1500 gaactgaaag tattgctacc tgaaccgttt atgacctttt cggattatct tgaagggatg 1560 tacgaggcag atgcaaagat cgagagagag agtgtctctg agttgctcgc ttccggtgat 1620 gatttgttca agaaaatcga tgagataaga aacaattaca gtggagtcga atttgatgta 1680 gagaaattcc aagaattttg caaggaactg aatgttaatc ctatgctaat tggccatgtc 1740 atcgaagcta ttttttcgca gaaggctggg gtaacagtaa cgggtctggg cacgctctct 1800 cctgagatgg gcgcttctgt tgcgttatcc agtacctctg tagatacatg tgaagatatg 1860 gatgtaactg aagatatgga ggatatagtg ttgatggcgg acaagagtca ttcttacatg 1920 tcccctgaaa tggcgagatg ggctgatgtt aaatatggca acaataaagg ggctctagtc 1980 gagtacaaag tcggaacctc gatgacttta cctgccacct gggcagagaa agttaaggct 2040 gtcttaccgt tgtcggggat ctgtgtgagg aaaccccaat tttcgaagcc gcttgatgag 2100 gaagatgact tgaggttatc aaacatgaat ttctttaagg tgagcgatct aaagttgaag 2160 aagactatca ctccagtcgt ttacactggg accattcgag agaggcaaat gaagaattat 2220 attgattact tatcggcctc tcttggttcc acgctgggta atctggagag aatcgtgcgg 2280 agtgattgga atggtactga ggagagtatg caaacgttcg ggttgtatga ctgcgaaaag 2340 tgcaagtggt tattgttgcc agccgagaag aagcacgcat gggccgtggt tctggcaagt 2400 gacgatacca ctcgcataat cttcctttca tatgacgaat ctggttctcc tataattgat 2460 aagaaaaact ggaagcgatt tgctgtctgt tccgagacca aagtctatag tgtaattcgt 2520 agcttagagg ttctaaataa ggaagcaata gtcgaccccg gggttcacat aacattagtt 2580 gacggagtgc cgggttgtgg aaagaccgcc gagattatag cgagggtcaa ttggaaaact 2640 gatctagtat tgactcccgg aagggaggca gctgctatga ttaggcggag agcctgcgcc 2700 ctgcacaagt cacctgtggc aaccaatgac aacgtcagaa ctttcgattc ttttgtgatg 2760 aataggaaaa tcttcaagtt tgacgctgtc tatgttgacg agggtctgat ggtccatacg 2820 ggattactta attttgcgtt aaagatctca ggttgtaaaa aagccttcgt ctttggtgat 2880 gctaagcaaa tcccgtttat aaacagagtc atgaatttcg attatcctaa ggagttaaga 2940 actttaatag tcgataatgt agagcgtagg tatgtcaccc ataggtgtcc tagagatgtc 3000 actagttttc ttaatactat ctataaagcc gctgtcgcta ctactagtcc ggttgtacat 3060 tctgtgaagg caattaaagt gtcaggggcc ggtattctga ggcctgagtt gacaaagatc 3120 aaaggaaaga taataacgtt tactcaatct gataagcagt ccttgatcaa gagtgggtac 3180 aatgatgtga atactgtgca tgaaattcag ggagaaacct ttgaggagac ggcagttgtg 3240 cgtgccaccc cgactccaat aggtttgatt gcccgtgatt caccacatgt actagtggcc 3300 ttaactaggc acactaaggc aatggtgtat tatactgttg tattcgatgc agttacaagt 3360 ataatagcgg atgtggaaaa ggtcgatcag tcgatcttga ccatgtttgc taccactgtg 3420 cctaccaaa 3429 18 1143 PRT Cucumber green mottle mosaic virus 129 kD replicase of CGMMV strain SH 18 Met Ala Asn Ile Asn Glu Gln Ile Asn Asn Gln Arg Asp Ala Ala Ala 1 5 10 15 Ser Gly Arg Asn Asn Leu Val Ser Gln Leu Ala Ser Lys Arg Val Tyr 20 25 30 Asp Glu Ala Val Arg Ser Leu Asp His Gln Asp Arg Arg Pro Lys Met 35 40 45 Asn Phe Ser Arg Val Val Ser Thr Glu His Thr Arg Leu Val Thr Asp 50 55 60 Ala Tyr Pro Glu Phe Ser Ile Ser Phe Thr Ala Thr Lys Asn Ser Val 65 70 75 80 His Ser Leu Ala Gly Gly Leu Arg Leu Leu Glu Leu Glu Tyr Met Met 85 90 95 Met Gln Val Pro Tyr Gly Ser Pro Cys Tyr Asp Ile Gly Gly Asn Tyr 100 105 110 Thr Gln His Leu Phe Lys Gly Arg Ser Tyr Val His Cys Cys Asn Pro 115 120 125 Cys Leu Asp Leu Lys Asp Val Ala Arg Asn Val Met Tyr Asn Asp Met 130 135 140 Ile Thr Gln His Val Gln Arg His Lys Gly Ser Cys Gly Cys Arg Pro 145 150 155 160 Leu Pro Thr Phe Gln Ile Asp Ala Phe Arg Arg Tyr Asp Ser Ser Pro 165 170 175 Cys Ala Val Thr Cys Ser Asp Val Phe Gln Glu Cys Ser Tyr Asp Phe 180 185 190 Gly Ser Gly Arg Asp Asn His Ala Val Ser Leu His Ser Ile Tyr Asp 195 200 205 Ile Pro Tyr Ser Ser Ile Gly Pro Ala Leu His Arg Lys Asn Val Arg 210 215 220 Val Cys Tyr Ala Ala Phe His Phe Ser Glu Ala Leu Leu Leu Gly Ser 225 230 235 240 Pro Val Gly Asn Leu Asn Ser Ile Gly Ala Gln Phe Arg Val Asp Gly 245 250 255 Asp Asp Val His Phe Leu Phe Ser Glu Glu Ser Thr Leu His Tyr Thr 260 265 270 His Ser Leu Glu Asn Ile Lys Leu Ile Val Met Arg Thr Tyr Phe Pro 275 280 285 Ala Asp Asp Arg Phe Val Tyr Ile Lys Glu Phe Met Val Lys Arg Val 290 295 300 Asp Thr Phe Phe Phe Arg Leu Val Arg Ala Asp Thr His Met Leu His 305 310 315 320 Lys Ser Val Gly His Tyr Ser Lys Ser Lys Ser Glu Tyr Phe Ala Leu 325 330 335 Asn Thr Pro Pro Ile Phe Gln Asp Lys Ala Thr Phe Ser Val Trp Phe 340 345 350 Pro Glu Ala Lys Lys Val Leu Ile Pro Lys Phe Glu Leu Ser Arg Phe 355 360 365 Leu Ser Gly Asn Val Lys Ile Ser Arg Met Leu Val Asp Ala Asp Phe 370 375 380 Val His Thr Ile Ile Asn His Ile Ser Thr Tyr Asp Asn Lys Ala Leu 385 390 395 400 Val Trp Lys Asn Val Gln Ser Phe Val Glu Ser Ile Arg Ser Arg Val 405 410 415 Ile Val Asn Gly Val Ser Val Lys Ser Glu Trp Asn Val Pro Val Asp 420 425 430 Gln Leu Thr Asp Ile Ser Phe Ser Ile Phe Pro Leu Val Lys Val Arg 435 440 445 Lys Val Gln Ile Glu Leu Met Ser Asp Lys Val Val Ile Glu Ala Arg 450 455 460 Gly Leu Leu Arg Arg Phe Ala Asp Ser Leu Lys Ser Ala Val Glu Gly 465 470 475 480 Leu Gly Asp Cys Val Tyr Asp Ala Leu Val Gln Thr Gly Trp Phe Asp 485 490 495 Thr Ser Ser Asp Glu Leu Lys Val Leu Leu Pro Glu Pro Phe Met Thr 500 505 510 Phe Ser Asp Tyr Leu Glu Gly Met Tyr Glu Ala Asp Ala Lys Ile Glu 515 520 525 Arg Glu Ser Val Ser Glu Leu Leu Ala Ser Gly Asp Asp Leu Phe Lys 530 535 540 Lys Ile Asp Glu Ile Arg Asn Asn Tyr Ser Gly Val Glu Phe Asp Val 545 550 555 560 Glu Lys Phe Gln Glu Phe Cys Lys Glu Leu Asn Val Asn Pro Met Leu 565 570 575 Ile Gly His Val Ile Glu Ala Ile Phe Ser Gln Lys Ala Gly Val Thr 580 585 590 Val Thr Gly Leu Gly Thr Leu Ser Pro Glu Met Gly Ala Ser Val Ala 595 600 605 Leu Ser Ser Thr Ser Val Asp Thr Cys Glu Asp Met Asp Val Thr Glu 610 615 620 Asp Met Glu Asp Ile Val Leu Met Ala Asp Lys Ser His Ser Tyr Met 625 630 635 640 Ser Pro Glu Met Ala Arg Trp Ala Asp Val Lys Tyr Gly Asn Asn Lys 645 650 655 Gly Ala Leu Val Glu Tyr Lys Val Gly Thr Ser Met Thr Leu Pro Ala 660 665 670 Thr Trp Ala Glu Lys Val Lys Ala Val Leu Pro Leu Ser Gly Ile Cys 675 680 685 Val Arg Lys Pro Gln Phe Ser Lys Pro Leu Asp Glu Glu Asp Asp Leu 690 695 700 Arg Leu Ser Asn Met Asn Phe Phe Lys Val Ser Asp Leu Lys Leu Lys 705 710 715 720 Lys Thr Ile Thr Pro Val Val Tyr Thr Gly Thr Ile Arg Glu Arg Gln 725 730 735 Met Lys Asn Tyr Ile Asp Tyr Leu Ser Ala Ser Leu Gly Ser Thr Leu 740 745 750 Gly Asn Leu Glu Arg Ile Val Arg Ser Asp Trp Asn Gly Thr Glu Glu 755 760 765 Ser Met Gln Thr Phe Gly Leu Tyr Asp Cys Glu Lys Cys Lys Trp Leu 770 775 780 Leu Leu Pro Ala Glu Lys Lys His Ala Trp Ala Val Val Leu Ala Ser 785 790 795 800 Asp Asp Thr Thr Arg Ile Ile Phe Leu Ser Tyr Asp Glu Ser Gly Ser 805 810 815 Pro Ile Ile Asp Lys Lys Asn Trp Lys Arg Phe Ala Val Cys Ser Glu 820 825 830 Thr Lys Val Tyr Ser Val Ile Arg Ser Leu Glu Val Leu Asn Lys Glu 835 840 845 Ala Ile Val Asp Pro Gly Val His Ile Thr Leu Val Asp Gly Val Pro 850 855 860 Gly Cys Gly Lys Thr Ala Glu Ile Ile Ala Arg Val Asn Trp Lys Thr 865 870 875 880 Asp Leu Val Leu Thr Pro Gly Arg Glu Ala Ala Ala Met Ile Arg Arg 885 890 895 Arg Ala Cys Ala Leu His Lys Ser Pro Val Ala Thr Asn Asp Asn Val 900 905 910 Arg Thr Phe Asp Ser Phe Val Met Asn Arg Lys Ile Phe Lys Phe Asp 915 920 925 Ala Val Tyr Val Asp Glu Gly Leu Met Val His Thr Gly Leu Leu Asn 930 935 940 Phe Ala Leu Lys Ile Ser Gly Cys Lys Lys Ala Phe Val Phe Gly Asp 945 950 955 960 Ala Lys Gln Ile Pro Phe Ile Asn Arg Val Met Asn Phe Asp Tyr Pro 965 970 975 Lys Glu Leu Arg Thr Leu Ile Val Asp Asn Val Glu Arg Arg Tyr Val 980 985 990 Thr His Arg Cys Pro Arg Asp Val Thr Ser Phe Leu Asn Thr Ile Tyr 995 1000 1005 Lys Ala Ala Val Ala Thr Thr Ser Pro Val Val His Ser Val Lys Ala 1010 1015 1020 Ile Lys Val Ser Gly Ala Gly Ile Leu Arg Pro Glu Leu Thr Lys Ile 1025 1030 1035 1040 Lys Gly Lys Ile Ile Thr Phe Thr Gln Ser Asp Lys Gln Ser Leu Ile 1045 1050 1055 Lys Ser Gly Tyr Asn Asp Val Asn Thr Val His Glu Ile Gln Gly Glu 1060 1065 1070 Thr Phe Glu Glu Thr Ala Val Val Arg Ala Thr Pro Thr Pro Ile Gly 1075 1080 1085 Leu Ile Ala Arg Asp Ser Pro His Val Leu Val Ala Leu Thr Arg His 1090 1095 1100 Thr Lys Ala Met Val Tyr Tyr Thr Val Val Phe Asp Ala Val Thr Ser 1105 1110 1115 1120 Ile Ile Ala Asp Val Glu Lys Val Asp Gln Ser Ile Leu Thr Met Phe 1125 1130 1135 Ala Thr Thr Val Pro Thr Lys 1140 19 1503 DNA Cucumber green mottle mosaic virus DNA sequence encoding 57 kD protein of CGMMV strain SH 19 atgcagaatt cgctgtatgt ccatcgtaat attttcctcc ctgttagtaa aacggggttt 60 tatacagaca tgcaggagtt ctacgataga tgccttcctg ggaattcctt cgtactaaat 120 gatttcgatg ccgtaaccat gcggttgagg gacaacgaat ttaacttaca accttgtagg 180 ctaaccttga gtaatttaga tccggtaccc gctttgatta agaatgaagc gcagaatttt 240 ctgatccccg ttttgcgtac ggcctgtgaa aggccgcgca ttccgggtct tcttgagaat 300 cttgtagcta tgataaagag gaatatgaat actcctgatt tagctgggac cgtagatata 360 actaacatgt cgatttctat agtagataac ttcttttctt cttttgttag ggacgaggtt 420 ttgcttgatc acttagattg tgttagggct agttccattc aaagtttttc tgattggttt 480 tcgtgtcaac caacctcagc ggttggccag ttagctaatt tcaatttcat agatttgcct 540 gcctttgata cttatatgca tatgattaag aggcaaccca agagtcggtt agatacttcg 600 attcagtctg aatatccggc cttgcaaact attgtttatc accctaaagt ggtaaatgca 660 gtttttggtc cggttttcaa gtatttaacc accaagtttc ttagtatggt agatagttct 720 aagtttttct tttacactag gaaaaaacca gaagatctgc aggaattttt ctcagatctc 780 tcttcccatt ctgattatga gattcttgag cttgatgttt ctaaatatga caagtcgcaa 840 tccgatttcc acttctctat tgagatggca atttgggaaa aattagggct tgacgatatt 900 ttggcttgga tgtggtctat gggtcacaaa agaactatac tgcaagattt ccaagccggg 960 ataaagacgc tcatttacta tcaacggaag tctggtgatg taactacttt tataggtaat 1020 acctttatta tcgcagcgtg tgtggctagt atgttgccgt tagataagtg ttttaaagct 1080 agtttttgtg gtgatgattc gctgatctac cttcctaagg gtttggagta tcctgatata 1140 caggctactg ccaaccttgt ttggaatttt gaggcgaaac ttttccgaaa gaagtatggt 1200 tacttctgcg ggaagtatat aattcaccat gccaacggct gtattgttta ccctgaccct 1260 ttaaaattaa ttagtaaatt aggtaataag agtcttgtag ggtatgagca tgttgaggag 1320 tttcgtatat ctctcctcga cgttgctcat agtttgttta atggtgctta tttccattta 1380 ctcgacgatg caatccacga attatttcct aatgctgggg gttgcagttt tgtaattaat 1440 tgtttgtgta agtatttgag tgataagcgc cttttccgta gtctttacat agatgtctct 1500 aag 1503 20 501 PRT Cucumber green mottle mosaic virus 57 kD protein of CGMMV strain SH 20 Met Gln Asn Ser Leu Tyr Val His Arg Asn Ile Phe Leu Pro Val Ser 1 5 10 15 Lys Thr Gly Phe Tyr Thr Asp Met Gln Glu Phe Tyr Asp Arg Cys Leu 20 25 30 Pro Gly Asn Ser Phe Val Leu Asn Asp Phe Asp Ala Val Thr Met Arg 35 40 45 Leu Arg Asp Asn Glu Phe Asn Leu Gln Pro Cys Arg Leu Thr Leu Ser 50 55 60 Asn Leu Asp Pro Val Pro Ala Leu Ile Lys Asn Glu Ala Gln Asn Phe 65 70 75 80 Leu Ile Pro Val Leu Arg Thr Ala Cys Glu Arg Pro Arg Ile Pro Gly 85 90 95 Leu Leu Glu Asn Leu Val Ala Met Ile Lys Arg Asn Met Asn Thr Pro 100 105 110 Asp Leu Ala Gly Thr Val Asp Ile Thr Asn Met Ser Ile Ser Ile Val 115 120 125 Asp Asn Phe Phe Ser Ser Phe Val Arg Asp Glu Val Leu Leu Asp His 130 135 140 Leu Asp Cys Val Arg Ala Ser Ser Ile Gln Ser Phe Ser Asp Trp Phe 145 150 155 160 Ser Cys Gln Pro Thr Ser Ala Val Gly Gln Leu Ala Asn Phe Asn Phe 165 170 175 Ile Asp Leu Pro Ala Phe Asp Thr Tyr Met His Met Ile Lys Arg Gln 180 185 190 Pro Lys Ser Arg Leu Asp Thr Ser Ile Gln Ser Glu Tyr Pro Ala Leu 195 200 205 Gln Thr Ile Val Tyr His Pro Lys Val Val Asn Ala Val Phe Gly Pro 210 215 220 Val Phe Lys Tyr Leu Thr Thr Lys Phe Leu Ser Met Val Asp Ser Ser 225 230 235 240 Lys Phe Phe Phe Tyr Thr Arg Lys Lys Pro Glu Asp Leu Gln Glu Phe 245 250 255 Phe Ser Asp Leu Ser Ser His Ser Asp Tyr Glu Ile Leu Glu Leu Asp 260 265 270 Val Ser Lys Tyr Asp Lys Ser Gln Ser Asp Phe His Phe Ser Ile Glu 275 280 285 Met Ala Ile Trp Glu Lys Leu Gly Leu Asp Asp Ile Leu Ala Trp Met 290 295 300 Trp Ser Met Gly His Lys Arg Thr Ile Leu Gln Asp Phe Gln Ala Gly 305 310 315 320 Ile Lys Thr Leu Ile Tyr Tyr Gln Arg Lys Ser Gly Asp Val Thr Thr 325 330 335 Phe Ile Gly Asn Thr Phe Ile Ile Ala Ala Cys Val Ala Ser Met Leu 340 345 350 Pro Leu Asp Lys Cys Phe Lys Ala Ser Phe Cys Gly Asp Asp Ser Leu 355 360 365 Ile Tyr Leu Pro Lys Gly Leu Glu Tyr Pro Asp Ile Gln Ala Thr Ala 370 375 380 Asn Leu Val Trp Asn Phe Glu Ala Lys Leu Phe Arg Lys Lys Tyr Gly 385 390 395 400 Tyr Phe Cys Gly Lys Tyr Ile Ile His His Ala Asn Gly Cys Ile Val 405 410 415 Tyr Pro Asp Pro Leu Lys Leu Ile Ser Lys Leu Gly Asn Lys Ser Leu 420 425 430 Val Gly Tyr Glu His Val Glu Glu Phe Arg Ile Ser Leu Leu Asp Val 435 440 445 Ala His Ser Leu Phe Asn Gly Ala Tyr Phe His Leu Leu Asp Asp Ala 450 455 460 Ile His Glu Leu Phe Pro Asn Ala Gly Gly Cys Ser Phe Val Ile Asn 465 470 475 480 Cys Leu Cys Lys Tyr Leu Ser Asp Lys Arg Leu Phe Arg Ser Leu Tyr 485 490 495 Ile Asp Val Ser Lys 500 21 4932 DNA Cucumber green mottle mosaic virus DNA sequence encoding 186 kD protein of CGMMV strain SH 21 atggcaaaca ttaatgaaca aatcaacaac caacgtgacg ccgcggctag cgggagaaac 60 aatctcgtta gccaattggc gtcaaaaagg gtgtatgacg aggctgttcg ctcgttggat 120 catcaagaca gacgcccgaa aatgaatttt tctcgtgtgg tcagcacaga gcacaccagg 180 cttgtaactg acgcgtatcc ggagttttcg attagcttta ccgccaccaa gaactctgta 240 cactcccttg cgggtggtct gaggcttctt gaattggaat atatgatgat gcaggtgccc 300 tacggctcac cttgttatga catcggcggt aactatacgc agcacttgtt caaaggtaga 360 tcatatgtgc attgctgcaa tccgtgccta gatcttaagg atgttgcgag gaatgtgatg 420 tacaacgata tgattacgca acatgtacag aggcacaagg gatcttgcgg gtgcagacct 480 cttccaactt tccagataga tgcattcagg aggtacgata gttctccctg tgcggtcacc 540 tgttcagacg ttttccaaga gtgttcctat gattttggga gtggtaggga taatcatgca 600 gtctcgttgc attcaatcta cgatatccct tattcttcga tcggacctgc tcttcatagg 660 aagaatgtgc gagtttgtta tgcagccttt catttctcgg aggcattgct tttaggttcg 720 cctgtaggta atttaaatag tattggggct cagtttaggg tcgatggtga tgatgtgcat 780 tttcttttta gtgaagagtc tactttgcat tatactcata gtttagaaaa tatcaagtta 840 atcgtgatgc gtacttactt tcctgctgat gataggtttg tatatattaa ggagttcatg 900 gttaagcgtg tggatacttt tttctttagg ttggtcagag cagatacaca catgcttcat 960 aaatctgtgg ggcactattc gaaatcgaag tctgagtact tcgcgctgaa tacccctccg 1020 atcttccaag ataaagccac gttttctgtg tggtttcctg aagcgaagaa ggtgttgata 1080 cccaagtttg aactttcgag attcctttct gggaatgtga aaatctctag gatgcttgtc 1140 gatgctgatt tcgtccatac cattattaat cacattagca cgtatgataa caaggcctta 1200 gtgtggaaga atgttcagtc ctttgtggaa tccatacgtt caagagtaat tgtaaacgga 1260 gtttccgtga aatctgagtg gaacgtaccg gttgatcagc tcactgatat ctcgttctcg 1320 atattccctc tcgtgaaggt taggaaggta cagatcgagt taatgtctga taaagttgta 1380 atcgaggcga ggggtttgct tcggaggttc gcagacagtc ttaaatctgc cgtagaagga 1440 ctaggtgatt gcgtctatga tgctctagtt caaaccggct ggtttgacac ctctagcgac 1500 gaactgaaag tattgctacc tgaaccgttt atgacctttt cggattatct tgaagggatg 1560 tacgaggcag atgcaaagat cgagagagag agtgtctctg agttgctcgc ttccggtgat 1620 gatttgttca agaaaatcga tgagataaga aacaattaca gtggagtcga atttgatgta 1680 gagaaattcc aagaattttg caaggaactg aatgttaatc ctatgctaat tggccatgtc 1740 atcgaagcta ttttttcgca gaaggctggg gtaacagtaa cgggtctggg cacgctctct 1800 cctgagatgg gcgcttctgt tgcgttatcc agtacctctg tagatacatg tgaagatatg 1860 gatgtaactg aagatatgga ggatatagtg ttgatggcgg acaagagtca ttcttacatg 1920 tcccctgaaa tggcgagatg ggctgatgtt aaatatggca acaataaagg ggctctagtc 1980 gagtacaaag tcggaacctc gatgacttta cctgccacct gggcagagaa agttaaggct 2040 gtcttaccgt tgtcggggat ctgtgtgagg aaaccccaat tttcgaagcc gcttgatgag 2100 gaagatgact tgaggttatc aaacatgaat ttctttaagg tgagcgatct aaagttgaag 2160 aagactatca ctccagtcgt ttacactggg accattcgag agaggcaaat gaagaattat 2220 attgattact tatcggcctc tcttggttcc acgctgggta atctggagag aatcgtgcgg 2280 agtgattgga atggtactga ggagagtatg caaacgttcg ggttgtatga ctgcgaaaag 2340 tgcaagtggt tattgttgcc agccgagaag aagcacgcat gggccgtggt tctggcaagt 2400 gacgatacca ctcgcataat cttcctttca tatgacgaat ctggttctcc tataattgat 2460 aagaaaaact ggaagcgatt tgctgtctgt tccgagacca aagtctatag tgtaattcgt 2520 agcttagagg ttctaaataa ggaagcaata gtcgaccccg gggttcacat aacattagtt 2580 gacggagtgc cgggttgtgg aaagaccgcc gagattatag cgagggtcaa ttggaaaact 2640 gatctagtat tgactcccgg aagggaggca gctgctatga ttaggcggag agcctgcgcc 2700 ctgcacaagt cacctgtggc aaccaatgac aacgtcagaa ctttcgattc ttttgtgatg 2760 aataggaaaa tcttcaagtt tgacgctgtc tatgttgacg agggtctgat ggtccatacg 2820 ggattactta attttgcgtt aaagatctca ggttgtaaaa aagccttcgt ctttggtgat 2880 gctaagcaaa tcccgtttat aaacagagtc atgaatttcg attatcctaa ggagttaaga 2940 actttaatag tcgataatgt agagcgtagg tatgtcaccc ataggtgtcc tagagatgtc 3000 actagttttc ttaatactat ctataaagcc gctgtcgcta ctactagtcc ggttgtacat 3060 tctgtgaagg caattaaagt gtcaggggcc ggtattctga ggcctgagtt gacaaagatc 3120 aaaggaaaga taataacgtt tactcaatct gataagcagt ccttgatcaa gagtgggtac 3180 aatgatgtga atactgtgca tgaaattcag ggagaaacct ttgaggagac ggcagttgtg 3240 cgtgccaccc cgactccaat aggtttgatt gcccgtgatt caccacatgt actagtggcc 3300 ttaactaggc acactaaggc aatggtgtat tatactgttg tattcgatgc agttacaagt 3360 ataatagcgg atgtggaaaa ggtcgatcag tcgatcttga ccatgtttgc taccactgtg 3420 cctaccaaaa tgcagaattc gctgtatgtc catcgtaata ttttcctccc tgttagtaaa 3480 acggggtttt atacagacat gcaggagttc tacgatagat gccttcctgg gaattccttc 3540 gtactaaatg atttcgatgc cgtaaccatg cggttgaggg acaacgaatt taacttacaa 3600 ccttgtaggc taaccttgag taatttagat ccggtacccg ctttgattaa gaatgaagcg 3660 cagaattttc tgatccccgt tttgcgtacg gcctgtgaaa ggccgcgcat tccgggtctt 3720 cttgagaatc ttgtagctat gataaagagg aatatgaata ctcctgattt agctgggacc 3780 gtagatataa ctaacatgtc gatttctata gtagataact tcttttcttc ttttgttagg 3840 gacgaggttt tgcttgatca cttagattgt gttagggcta gttccattca aagtttttct 3900 gattggtttt cgtgtcaacc aacctcagcg gttggccagt tagctaattt caatttcata 3960 gatttgcctg cctttgatac ttatatgcat atgattaaga ggcaacccaa gagtcggtta 4020 gatacttcga ttcagtctga atatccggcc ttgcaaacta ttgtttatca ccctaaagtg 4080 gtaaatgcag tttttggtcc ggttttcaag tatttaacca ccaagtttct tagtatggta 4140 gatagttcta agtttttctt ttacactagg aaaaaaccag aagatctgca ggaatttttc 4200 tcagatctct cttcccattc tgattatgag attcttgagc ttgatgtttc taaatatgac 4260 aagtcgcaat ccgatttcca cttctctatt gagatggcaa tttgggaaaa attagggctt 4320 gacgatattt tggcttggat gtggtctatg ggtcacaaaa gaactatact gcaagatttc 4380 caagccggga taaagacgct catttactat caacggaagt ctggtgatgt aactactttt 4440 ataggtaata cctttattat cgcagcgtgt gtggctagta tgttgccgtt agataagtgt 4500 tttaaagcta gtttttgtgg tgatgattcg ctgatctacc ttcctaaggg tttggagtat 4560 cctgatatac aggctactgc caaccttgtt tggaattttg aggcgaaact tttccgaaag 4620 aagtatggtt acttctgcgg gaagtatata attcaccatg ccaacggctg tattgtttac 4680 cctgaccctt taaaattaat tagtaaatta ggtaataaga gtcttgtagg gtatgagcat 4740 gttgaggagt ttcgtatatc tctcctcgac gttgctcata gtttgtttaa tggtgcttat 4800 ttccatttac tcgacgatgc aatccacgaa ttatttccta atgctggggg ttgcagtttt 4860 gtaattaatt gtttgtgtaa gtatttgagt gataagcgcc ttttccgtag tctttacata 4920 gatgtctcta ag 4932 22 1644 PRT Cucumber green mottle mosaic virus 186 kD protein of CGMMV strain SH 22 Met Ala Asn Ile Asn Glu Gln Ile Asn Asn Gln Arg Asp Ala Ala Ala 1 5 10 15 Ser Gly Arg Asn Asn Leu Val Ser Gln Leu Ala Ser Lys Arg Val Tyr 20 25 30 Asp Glu Ala Val Arg Ser Leu Asp His Gln Asp Arg Arg Pro Lys Met 35 40 45 Asn Phe Ser Arg Val Val Ser Thr Glu His Thr Arg Leu Val Thr Asp 50 55 60 Ala Tyr Pro Glu Phe Ser Ile Ser Phe Thr Ala Thr Lys Asn Ser Val 65 70 75 80 His Ser Leu Ala Gly Gly Leu Arg Leu Leu Glu Leu Glu Tyr Met Met 85 90 95 Met Gln Val Pro Tyr Gly Ser Pro Cys Tyr Asp Ile Gly Gly Asn Tyr 100 105 110 Thr Gln His Leu Phe Lys Gly Arg Ser Tyr Val His Cys Cys Asn Pro 115 120 125 Cys Leu Asp Leu Lys Asp Val Ala Arg Asn Val Met Tyr Asn Asp Met 130 135 140 Ile Thr Gln His Val Gln Arg His Lys Gly Ser Cys Gly Cys Arg Pro 145 150 155 160 Leu Pro Thr Phe Gln Ile Asp Ala Phe Arg Arg Tyr Asp Ser Ser Pro 165 170 175 Cys Ala Val Thr Cys Ser Asp Val Phe Gln Glu Cys Ser Tyr Asp Phe 180 185 190 Gly Ser Gly Arg Asp Asn His Ala Val Ser Leu His Ser Ile Tyr Asp 195 200 205 Ile Pro Tyr Ser Ser Ile Gly Pro Ala Leu His Arg Lys Asn Val Arg 210 215 220 Val Cys Tyr Ala Ala Phe His Phe Ser Glu Ala Leu Leu Leu Gly Ser 225 230 235 240 Pro Val Gly Asn Leu Asn Ser Ile Gly Ala Gln Phe Arg Val Asp Gly 245 250 255 Asp Asp Val His Phe Leu Phe Ser Glu Glu Ser Thr Leu His Tyr Thr 260 265 270 His Ser Leu Glu Asn Ile Lys Leu Ile Val Met Arg Thr Tyr Phe Pro 275 280 285 Ala Asp Asp Arg Phe Val Tyr Ile Lys Glu Phe Met Val Lys Arg Val 290 295 300 Asp Thr Phe Phe Phe Arg Leu Val Arg Ala Asp Thr His Met Leu His 305 310 315 320 Lys Ser Val Gly His Tyr Ser Lys Ser Lys Ser Glu Tyr Phe Ala Leu 325 330 335 Asn Thr Pro Pro Ile Phe Gln Asp Lys Ala Thr Phe Ser Val Trp Phe 340 345 350 Pro Glu Ala Lys Lys Val Leu Ile Pro Lys Phe Glu Leu Ser Arg Phe 355 360 365 Leu Ser Gly Asn Val Lys Ile Ser Arg Met Leu Val Asp Ala Asp Phe 370 375 380 Val His Thr Ile Ile Asn His Ile Ser Thr Tyr Asp Asn Lys Ala Leu 385 390 395 400 Val Trp Lys Asn Val Gln Ser Phe Val Glu Ser Ile Arg Ser Arg Val 405 410 415 Ile Val Asn Gly Val Ser Val Lys Ser Glu Trp Asn Val Pro Val Asp 420 425 430 Gln Leu Thr Asp Ile Ser Phe Ser Ile Phe Pro Leu Val Lys Val Arg 435 440 445 Lys Val Gln Ile Glu Leu Met Ser Asp Lys Val Val Ile Glu Ala Arg 450 455 460 Gly Leu Leu Arg Arg Phe Ala Asp Ser Leu Lys Ser Ala Val Glu Gly 465 470 475 480 Leu Gly Asp Cys Val Tyr Asp Ala Leu Val Gln Thr Gly Trp Phe Asp 485 490 495 Thr Ser Ser Asp Glu Leu Lys Val Leu Leu Pro Glu Pro Phe Met Thr 500 505 510 Phe Ser Asp Tyr Leu Glu Gly Met Tyr Glu Ala Asp Ala Lys Ile Glu 515 520 525 Arg Glu Ser Val Ser Glu Leu Leu Ala Ser Gly Asp Asp Leu Phe Lys 530 535 540 Lys Ile Asp Glu Ile Arg Asn Asn Tyr Ser Gly Val Glu Phe Asp Val 545 550 555 560 Glu Lys Phe Gln Glu Phe Cys Lys Glu Leu Asn Val Asn Pro Met Leu 565 570 575 Ile Gly His Val Ile Glu Ala Ile Phe Ser Gln Lys Ala Gly Val Thr 580 585 590 Val Thr Gly Leu Gly Thr Leu Ser Pro Glu Met Gly Ala Ser Val Ala 595 600 605 Leu Ser Ser Thr Ser Val Asp Thr Cys Glu Asp Met Asp Val Thr Glu 610 615 620 Asp Met Glu Asp Ile Val Leu Met Ala Asp Lys Ser His Ser Tyr Met 625 630 635 640 Ser Pro Glu Met Ala Arg Trp Ala Asp Val Lys Tyr Gly Asn Asn Lys 645 650 655 Gly Ala Leu Val Glu Tyr Lys Val Gly Thr Ser Met Thr Leu Pro Ala 660 665 670 Thr Trp Ala Glu Lys Val Lys Ala Val Leu Pro Leu Ser Gly Ile Cys 675 680 685 Val Arg Lys Pro Gln Phe Ser Lys Pro Leu Asp Glu Glu Asp Asp Leu 690 695 700 Arg Leu Ser Asn Met Asn Phe Phe Lys Val Ser Asp Leu Lys Leu Lys 705 710 715 720 Lys Thr Ile Thr Pro Val Val Tyr Thr Gly Thr Ile Arg Glu Arg Gln 725 730 735 Met Lys Asn Tyr Ile Asp Tyr Leu Ser Ala Ser Leu Gly Ser Thr Leu 740 745 750 Gly Asn Leu Glu Arg Ile Val Arg Ser Asp Trp Asn Gly Thr Glu Glu 755 760 765 Ser Met Gln Thr Phe Gly Leu Tyr Asp Cys Glu Lys Cys Lys Trp Leu 770 775 780 Leu Leu Pro Ala Glu Lys Lys His Ala Trp Ala Val Val Leu Ala Ser 785 790 795 800 Asp Asp Thr Thr Arg Ile Ile Phe Leu Ser Tyr Asp Glu Ser Gly Ser 805 810 815 Pro Ile Ile Asp Lys Lys Asn Trp Lys Arg Phe Ala Val Cys Ser Glu 820 825 830 Thr Lys Val Tyr Ser Val Ile Arg Ser Leu Glu Val Leu Asn Lys Glu 835 840 845 Ala Ile Val Asp Pro Gly Val His Ile Thr Leu Val Asp Gly Val Pro 850 855 860 Gly Cys Gly Lys Thr Ala Glu Ile Ile Ala Arg Val Asn Trp Lys Thr 865 870 875 880 Asp Leu Val Leu Thr Pro Gly Arg Glu Ala Ala Ala Met Ile Arg Arg 885 890 895 Arg Ala Cys Ala Leu His Lys Ser Pro Val Ala Thr Asn Asp Asn Val 900 905 910 Arg Thr Phe Asp Ser Phe Val Met Asn Arg Lys Ile Phe Lys Phe Asp 915 920 925 Ala Val Tyr Val Asp Glu Gly Leu Met Val His Thr Gly Leu Leu Asn 930 935 940 Phe Ala Leu Lys Ile Ser Gly Cys Lys Lys Ala Phe Val Phe Gly Asp 945 950 955 960 Ala Lys Gln Ile Pro Phe Ile Asn Arg Val Met Asn Phe Asp Tyr Pro 965 970 975 Lys Glu Leu Arg Thr Leu Ile Val Asp Asn Val Glu Arg Arg Tyr Val 980 985 990 Thr His Arg Cys Pro Arg Asp Val Thr Ser Phe Leu Asn Thr Ile Tyr 995 1000 1005 Lys Ala Ala Val Ala Thr Thr Ser Pro Val Val His Ser Val Lys Ala 1010 1015 1020 Ile Lys Val Ser Gly Ala Gly Ile Leu Arg Pro Glu Leu Thr Lys Ile 1025 1030 1035 1040 Lys Gly Lys Ile Ile Thr Phe Thr Gln Ser Asp Lys Gln Ser Leu Ile 1045 1050 1055 Lys Ser Gly Tyr Asn Asp Val Asn Thr Val His Glu Ile Gln Gly Glu 1060 1065 1070 Thr Phe Glu Glu Thr Ala Val Val Arg Ala Thr Pro Thr Pro Ile Gly 1075 1080 1085 Leu Ile Ala Arg Asp Ser Pro His Val Leu Val Ala Leu Thr Arg His 1090 1095 1100 Thr Lys Ala Met Val Tyr Tyr Thr Val Val Phe Asp Ala Val Thr Ser 1105 1110 1115 1120 Ile Ile Ala Asp Val Glu Lys Val Asp Gln Ser Ile Leu Thr Met Phe 1125 1130 1135 Ala Thr Thr Val Pro Thr Lys Met Gln Asn Ser Leu Tyr Val His Arg 1140 1145 1150 Asn Ile Phe Leu Pro Val Ser Lys Thr Gly Phe Tyr Thr Asp Met Gln 1155 1160 1165 Glu Phe Tyr Asp Arg Cys Leu Pro Gly Asn Ser Phe Val Leu Asn Asp 1170 1175 1180 Phe Asp Ala Val Thr Met Arg Leu Arg Asp Asn Glu Phe Asn Leu Gln 1185 1190 1195 1200 Pro Cys Arg Leu Thr Leu Ser Asn Leu Asp Pro Val Pro Ala Leu Ile 1205 1210 1215 Lys Asn Glu Ala Gln Asn Phe Leu Ile Pro Val Leu Arg Thr Ala Cys 1220 1225 1230 Glu Arg Pro Arg Ile Pro Gly Leu Leu Glu Asn Leu Val Ala Met Ile 1235 1240 1245 Lys Arg Asn Met Asn Thr Pro Asp Leu Ala Gly Thr Val Asp Ile Thr 1250 1255 1260 Asn Met Ser Ile Ser Ile Val Asp Asn Phe Phe Ser Ser Phe Val Arg 1265 1270 1275 1280 Asp Glu Val Leu Leu Asp His Leu Asp Cys Val Arg Ala Ser Ser Ile 1285 1290 1295 Gln Ser Phe Ser Asp Trp Phe Ser Cys Gln Pro Thr Ser Ala Val Gly 1300 1305 1310 Gln Leu Ala Asn Phe Asn Phe Ile Asp Leu Pro Ala Phe Asp Thr Tyr 1315 1320 1325 Met His Met Ile Lys Arg Gln Pro Lys Ser Arg Leu Asp Thr Ser Ile 1330 1335 1340 Gln Ser Glu Tyr Pro Ala Leu Gln Thr Ile Val Tyr His Pro Lys Val 1345 1350 1355 1360 Val Asn Ala Val Phe Gly Pro Val Phe Lys Tyr Leu Thr Thr Lys Phe 1365 1370 1375 Leu Ser Met Val Asp Ser Ser Lys Phe Phe Phe Tyr Thr Arg Lys Lys 1380 1385 1390 Pro Glu Asp Leu Gln Glu Phe Phe Ser Asp Leu Ser Ser His Ser Asp 1395 1400 1405 Tyr Glu Ile Leu Glu Leu Asp Val Ser Lys Tyr Asp Lys Ser Gln Ser 1410 1415 1420 Asp Phe His Phe Ser Ile Glu Met Ala Ile Trp Glu Lys Leu Gly Leu 1425 1430 1435 1440 Asp Asp Ile Leu Ala Trp Met Trp Ser Met Gly His Lys Arg Thr Ile 1445 1450 1455 Leu Gln Asp Phe Gln Ala Gly Ile Lys Thr Leu Ile Tyr Tyr Gln Arg 1460 1465 1470 Lys Ser Gly Asp Val Thr Thr Phe Ile Gly Asn Thr Phe Ile Ile Ala 1475 1480 1485 Ala Cys Val Ala Ser Met Leu Pro Leu Asp Lys Cys Phe Lys Ala Ser 1490 1495 1500 Phe Cys Gly Asp Asp Ser Leu Ile Tyr Leu Pro Lys Gly Leu Glu Tyr 1505 1510 1515 1520 Pro Asp Ile Gln Ala Thr Ala Asn Leu Val Trp Asn Phe Glu Ala Lys 1525 1530 1535 Leu Phe Arg Lys Lys Tyr Gly Tyr Phe Cys Gly Lys Tyr Ile Ile His 1540 1545 1550 His Ala Asn Gly Cys Ile Val Tyr Pro Asp Pro Leu Lys Leu Ile Ser 1555 1560 1565 Lys Leu Gly Asn Lys Ser Leu Val Gly Tyr Glu His Val Glu Glu Phe 1570 1575 1580 Arg Ile Ser Leu Leu Asp Val Ala His Ser Leu Phe Asn Gly Ala Tyr 1585 1590 1595 1600 Phe His Leu Leu Asp Asp Ala Ile His Glu Leu Phe Pro Asn Ala Gly 1605 1610 1615 Gly Cys Ser Phe Val Ile Asn Cys Leu Cys Lys Tyr Leu Ser Asp Lys 1620 1625 1630 Arg Leu Phe Arg Ser Leu Tyr Ile Asp Val Ser Lys 1635 1640 23 1139 DNA Cucumber green mottle mosaic virus DNA sequnece encoding coat protein of CGMMV strain SH 23 aattcggctt ctgtaggggt ggtgctactg ttgctctggt tgacacaagg atgcattctg 60 ttgcagaggg aactatatgc aaattttcag ctcccgccac cgtccgcgaa ttctctgtta 120 ggttcatacc taattatcct gtcgtggctg cggatgccct tcgcgatcct tggtctttat 180 ttgtgagact ctctaatgtg ggcattaaag atggtttcca tcctttgact ttagaggtcg 240 cttgtttagt cgctacaact aactctatta tcaaaaaggg tcttagagct tctgtagtcg 300 agtctgtcgt ctcttccgat cagtctattg tcctagattc cttgtccgag aaagttgaac 360 ctttctttga caaagttcct atttcagcgg ctgtaatggc aagagatccc agttataggt 420 ctaggtcaca gtctgtcggt ggtcgtggta agcggcattc taaacctcca aatcggaggt 480 tggactctgc ttctgaagag tccagttctg tttcttttga agatggctta caatccgatc 540 acacctagca aacttattgc gtttagtgct tcatatgttc ccgtcaggac tttacttaat 600 tttctagttg cttcacaagg taccgctttt cagactcaag cgggaagaga ttctttccgc 660 gagtccctgt ctgcgttacc ctcgtctgtc gtagatatta attctagatt cccagatgcg 720 ggtttttacg ctttcctcaa cggtcctgtg ttgaggccta tcttcgtttc gcttctcagc 780 tccacggata cgcgtaatag ggtcattgag gttgtagatc ctagcaatcc tacgactgct 840 gagtcgctta acgctgtaaa gcgtactgat gacgcgtcta cagccgctag ggccgagata 900 gataatttaa tagagtctat ttctaagggt tttgatgttt acgatagggc ttcatttgaa 960 gccgcgtttt cggtagtctg gtcagaggct accacctcga aagcttagtt tcgagggtct 1020 tctgatggtg gtgcacacca aagtgcatag tgctttcccg ttcacttaaa tcgaacggtt 1080 tgctcattgg tttgcggaaa cctctcacgt gtgacgttga agtttctatg ggcaagccg 1139 24 24 DNA Artificial Sequence Description of Artificial Sequence primer 97G01 24 aggtgtcagt ggagaactca ttga 24 25 17 DNA Artificial Sequence Description of Artificial Sequence primer 97G02 25 ggcgttgtgg tttgtgg 17 26 21 DNA Artificial Sequence Description of Artificial Sequence primer 97G03 26 ctgtaggggt ggtgctactg t 21 27 21 DNA Artificial Sequence Description of Artificial Sequence primer 97G18 27 gcccatagaa acttcaacgt c 21 28 24 DNA Artificial Sequence Description of Artificial Sequence primer 98A88 28 ccatggagaa ttcgctgtat gtcc 24 29 23 DNA Artificial Sequence Description of Artificial Sequence primer 98A86 29 cgagctctcg actgacacct tac 23 30 21 DNA Artificial Sequence Description of Artificial Sequence primer 98A84 30 ccatggcaaa cattaatgaa c 21 31 21 DNA Artificial Sequence Description of Artificial Sequence primer 98A85 31 caaccatggc aaacattaat g 21 32 22 DNA Artificial Sequence Description of Artificial Sequence primer 98G63 32 taacagggag gaaaatatta cg 22 33 24 DNA Artificial Sequence Description of Artificial Sequence primer 98L99 33 gagctcggat ccactagtaa cggc 24 34 28 DNA Artificial Sequence Description of Artificial Sequence primer 98L107 34 tagagctctt gaagctaagc aaattccg 28 35 31 DNA Artificial Sequence Description of Artificial Sequence primer 98L108 35 ttcaagagct ctaatcaccg aagacaaagg c 31 36 24 DNA Artificial Sequence Description of Artificial Sequence primer 98L102 36 gaattatatc gattatctat cggc 24 37 27 DNA Artificial Sequence Description of Artificial Sequence primer 98L103 37 gataatcgat ataattcttc atctgcc 27 38 29 DNA Artificial Sequence Description of Artificial Sequence primer 98L104 38 aactagtaat tgatgatctg ttcaagaag 29 39 31 DNA Artificial Sequence Description of Artificial Sequence primer 98L105 39 aattactagt ttccggaagc aagcagctca g 31 40 22 DNA Artificial Sequence Description of Artificial Sequence primer 98L106 40 gccctctaga tgcatgctcg ag 22 41 30 DNA Artificial Sequence Description of Artificial Sequence primer 97G40 41 ctagagtttt aatttttata attaaacaaa 30 42 36 DNA Artificial Sequence Description of Artificial Sequence primer 97G41 42 tcaaaattaa aaatattaat ttgtttgttg ttgttg 36 43 36 DNA Artificial Sequence Description of Artificial Sequence primer 97G42 43 caacaacaac aacaacaaac aattttaaaa caacac 36 44 30 DNA Artificial Sequence Description of Artificial Sequence primer 97G43 44 ttgttgtttg ttaaaatttt gttgtggtac 30 45 22 DNA Artificial Sequence Description of Artificial Sequence primer 1 45 cgagctcatc tcgttagtca gc 22 46 20 DNA Artificial Sequence Description of Artificial Sequence primer 2 46 gggatccacg tctggacagg 20 47 22 DNA Artificial Sequence Description of Artificial Sequence primer 3 47 ctctagaatc tcgttagtca gc 22 48 21 DNA Artificial Sequence Description of Artificial Sequence primer 4 48 aggatcctac acgaacctat c 21 49 23 DNA Artificial Sequence Description of Artificial Sequence primer 5 49 aggatccatt gcggtaacac aac 23 50 23 DNA Artificial Sequence Description of Artificial Sequence primer 6 50 tagatctatt gcggtaacac aac 23 51 19 DNA Artificial Sequence Description of Artificial Sequence primer 7 51 tagatctgtg tgattctgg 19 52 19 DNA Artificial Sequence Description of Artificial Sequence primer 8 52 aggatccgtg tgattctgg 19 53 22 DNA Artificial Sequence Description of Artificial Sequence primer 9 53 aggatccgtg tacgtaagtt tc 22 54 22 DNA Artificial Sequence Description of Artificial Sequence primer 10 54 tagatctgtg tacgtaagtt tc 22 55 20 DNA Artificial Sequence Description of Artificial Sequence primer 11 55 tagatctgtg atacctgcag 20 56 20 DNA Artificial Sequence Description of Artificial Sequence primer 12 56 aggatccgtg atacctgcag 20 57 26 DNA Artificial Sequence Description of Artificial Sequence primer 13 57 cgagctcatc tcgttagtca gctagc 26 58 25 DNA Artificial Sequence Description of Artificial Sequence primer 14 58 aggatccttt gtgcctctgt acatg 25 59 26 DNA Artificial Sequence Description of Artificial Sequence primer 15 59 ctctagaatc tcgttagtca gctagc 26 60 26 DNA Artificial Sequence Description of Artificial Sequence primer 16 60 aggatccatc aaccctaaat tgagcc 26 61 26 DNA Artificial Sequence Description of Artificial Sequence primer 17 61 aggatccagc agggaaataa gtacgc 26 62 25 DNA Artificial Sequence Description of Artificial Sequence primer 18 62 aggatccggt atggacaaaa tcagc 25 63 28 DNA Artificial Sequence Description of Artificial Sequence primer 19 63 aggatccatt gcggtaacac aacctctc 28 64 24 DNA Artificial Sequence Description of Artificial Sequence primer 20 64 tagatctgtg tgattctgga aaag 24 65 26 DNA Artificial Sequence Description of Artificial Sequence primer 21 65 tagatctgtg atacctgcac atcaac 26 66 28 DNA Artificial Sequence Description of Artificial Sequence primer 22 66 aggatccgtg tacgtaagtt tctgcttc 28 67 26 DNA Artificial Sequence Description of Artificial Sequence primer 23 67 ctctagaatc tcgttagtca gctagc 26 68 26 DNA Artificial Sequence Description of Artificial Sequence primer 24 68 aggatccagc agggaaataa gtacgc 26 

1. A method for generating Estate in a plant or in a plant cell against infection with CGMMV, said method comprising at least the step of providing, preferably transforming said plant or plant cell with a polynucleotide sequence that upon (at least) transformation into a plant and transcription into RNA generates resistance against infection with CGMMV in said plant; optionally upon (at least) transformation into a plant and transcription into RNA does not lead to generation of (any) replicase activity in said plant; and wherein the polynucleotide sequence comprises a first and a second DNA sequence, wherein: the first DNA sequence comprises a promoter, operably linked to a first DNA region capable of being transcribed into a sense RNA molecule with a nucleotide sequence comprising a sense nucleotide sequence of at least 10 consecutive nucleotides having between 75 and 100% sequence identity with at least part of the nucleotide sequence of the genome of the CGMMV virus, capable of infecting the plant or the plant cell; optionally a DNA region involved in transcription termination and polyadenylation functioning in plant cells and wherein the second chimeric DNA comprises a promoter, operably linked to a second DNA region capable of being transcribed into an antisense RNA molecule with a nucleotide sequence comprising an antisense nucleotide sequence including at least 10 consecutive nucleotides, hang between about 75% to about 100% secquence identity with the complment of at least IO cousecutive nucleotides of the sense nucleotide sequence; and optionally a DNA region involved in transcription termination and polyadenylation functioning in plant cells and wherein the sense and antisense RNA molecules are capable of forming a double stranded RNA region by base-pairing between the regions which are complementary.
 2. The method according to claim 1, wherein the cells of the plants are provided with the first and second DNA sequence by crossing parent plants comprising either be first or the second DNA sequence.
 3. The method according to claim 1, wherein the cells of the plants are provided with the first and second DNA sequence by transforming a plant cell with the first and second DNA sequence and regenerating a plant from the transformed plant cell.
 4. The method according to claim 1, wherein the first and second DNA sequence are integrated separately in the nuclear genome of the plant cell.
 5. The method according to claim 1, in which the polynucleotide sequence is derived from a nucleotide sequence that comprises, and preferably consists of: at least part of one of the nucleotide sequence corresponding to the sequence given in SEQ ID no.1, to the sequence given in SEQ ED no.17 or to the nucleotide sequence of a naturally occurring variant thereof; at least part of one of a nucleotide sequence corresponding to the sequence given in SEQ ID no.5, to the sequence given in SEQ ID no.21, to the nucleotide sequence of a naturally occurring variant thereof; at least part of one of a nucleotide sequence corresponding to the sequence given in SEQ ID no.3, to the sequence given in SEQ ID no.19 or to the nucleotide sequence of a naturally occurring variant thereof; such that said nucleotide sequence is capable, upon (at least) information into a plant and transition into RNA, to confer to said plant resistance against infection with CGMMV.
 6. Method according to claim 5, wherein the polynucleotide sequence encodes for an inverted repeat RNA Sequence optionally linked by a spacer and wherein the spacer is preferably an intron.
 7. Method according to any of the claims 1-6, further comprising at least one step of cultivating the transformed plant cell into a mature plant.
 8. Method according to any of the claims 1-7, further comprising at least one step of sexually or asexually reproducing or multiplying the transformed plant and/or the mature plant obtained from the transformed plant cell of claim
 7. 9. Method according to any of the claims 1-8, in which the plant is a plant that is susceptible to infection with CCMMV, more preferably a plant belonging to the Cucurbitaceae family, such as melon (Cucumis melo), cucumber (C. sativus), watermelon (Citrullus vulgaris) and bottlegourd (Lagenaria siceraria).
 10. Genetic construct suitable for transforming a plant, said construct at least comprising nucleotide sequence that upon (at least) transformation into a plant and transcription into RNA generates resistance against infection with CGMMV in said plant; and optionally upon (at least) transformation into a plant and transcription into RNA does not lead to generation of (any) replicase activity in said plant; and optionally comprising further elements of genetic constructs known per se.
 11. Genetic construct according to claims 10, in which the nucleotide sequence is under control of the plastocyanine-promoter.
 12. Genetic compact according to claim 10 or 11 in a form that can be stably maintained or inherited in a micro-orgaism, in particular a bacterium, more in particular a bacterium that can be used to transform a plant or plant materials such as Agrobacterium.
 13. Micro-organism, in particular bacterium, more in particular a bacterium that can be used to transform a plant, such as Agrobacterium, that contains a genetic construct according to any of claims 10-12, and in particular according to claim
 12. 14. Transgenic plant or plant cell, obtainable or obtained by a method according to one of claims 1-9, or a descendant of such a plant.
 15. Plant, plant cell or plant material that has been transformed with genetic construct according to any of claims 1-9, or a descendant of such a plant.
 16. Plant according to claim 14 or 15, being a plant that is susceptible to infection with CGMMV, more preferably a plant belonging to the Cucurbitaceae family, such as melon (Cucumis melo), cucumber (C. sativus), watermelon (Citrullus vulgaris) and bottlegourd (Lagenaria siceraria).
 17. Cultivation material such as seed, tubers, roots, stalks, seedlings for a plant according to claim 14, 15 or
 16. 18. Method for generating resistance in a plant or in a plant cell against infection with CGMMV, said method comprising at least the step of transforming said plant or plant cell with a polynucleotide sequence that upon (at least) transformation into a plant and transcription into RNA generates resistance against infection with CGMMV in said plant; and upon (at least) transformation into a plant and transcription into RNA does not lead to generation of (any) replicase activity in said plant.
 19. Method for providing a transgenic plant and/or a transgenic plant cell that is resist against infection with CGMMV, comprising at least the step of transforming said plant or plant cell with a polynucleotide sequence that upon (at least) transformation into a plant and transcription into RNA generates resistance against infection with CGMMV in said plant; and upon (at least) transformation into a plant and transcription into RNA does not lead to generation of (any) replicase activity in said plant.
 20. Method according to claim 18 and/or 19, in which the polynucleotide sequence is a nucleotide sequence that comprises, and preferably consists of: a nucleotide sequence corresponding to the sequence given in SEQ ID no.1, to the sequence given in SEQ ID no.17 or to the nucleotide sequence of a natrually occurring variant thereof in which—compared to the sequence of SEQ D no.1, SEQ ID no. 17 and/or the naturally occurring variant thereof—one or more nucleotides have been added, replaced and/or removed; a nucleotide sequence corresponding to the sequence given in SEQ ID to.5, to the sequence given in SEQ ID no21, to the nucleotide sequence of a naturally occurring variant thereof, in which—compared to the sequence of SEQ ID no.5, SEQ no. 21 and/or the naturally occurring variant thereof one or more nucleotides have been added, replaced and/or removed; a nucleotide sequence corresponding to the sequence given in SEQ ID no.3, to the sequence given in SEQ ID no.19 or to the nucleotide sequence of a naturally occuring variant thereof; a nucleotide sequence corresponding to the sequence give in SEQ ID no.3, to the sequence given in SEQ ID no.19 or to the nucleotide sequence of a naturally occurring variant thereof, in which—compared to the sequence of SEQ ID no.3, SEQ ID No. 19 and/or the naturally occuring vast thereof—one or more nucleotides have been added, replaced and/or removed; such that said nucleotide sequence is capable, upon (at least) transformation into a plant and transcription into RNA, to confer to said plant resistance against infection with CGMMV, and such that said nucleotide sequence, upon (at least) transformation into a plant and transcription into RNA, is not capable of generating of (any) replicase activity in said plant.
 21. Method according to any of claims 18-20, in which the polynucleotide sequence encodes a polypeptide or protein that upon by expressed in a plant is capable of generating resistance against CGMMV in said plant; and upon being expressed in a plant has no replicase activity.
 22. Method according to claim 21, in which the polynucleotide sequence encodes a protein or polypeptide that comprises, and preferably consists of: an amino acid sequence corresponding to the sequence given in SEQ ED no.2, to the sequence given in SEQ ID no.18 or to the amino acid sequence of a mutually occuring variant thereof, in which—compared to the sequence of SEQ ID no.2, SEQ ID no.18 and/or the naturally occuring variant thereof—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed; an amino acid sequence corresponding to the sequence given in SEQ ID no.6, to the sequence given in SEQ ID no.22 or to the amino acid sequence of a naturally occur variant thereon in which—compared to the sequence of SEQ ID no.6, SEQ ID no. 22 and/or the naturally occuring variant thereof—one or more ammo acids have been added, replaced or removed, preferably replaced or removed, more preferably removed an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no.20 or to the ammo acid sequence of a naturally occuring variant thereof; an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no.20 or to the amino acid sequence of a naturally occuring variant thereof in which—compared to the sequence of SEQ ID no.4, SEQ ID no. 20 and/or the naturally occuring variant thereof—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed; or any combination thereof, provided that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to generate resistance against CGMMV in said plant.
 23. Method according to claim 21 or 22, in which the polynucleotide sequence encodes a protein or polypeptide that comprises, and preferably consists of an amino acid sequence corresponding to a part or fragment of tie sequence given in SEQ ID no.2, to a part or fragment of the sequence given in SEQ D no.18 and/or to a part of fragment of the amino acid sequence of a naturally occuring variant thereof, or corresponding to a combination of two or more such parts or fragments; an amino acid sequence corresponding to a part or fragment of the sequence given in SEQ ID no.6, to a part or fragment of the sequence given in SEQ ID no.22 and/or to a part of fragment of the amino acid sequence of a naturally occuring variant thereof, or corresponding to a combination of two or more such parts or fragments; an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no.20, and/or to the amino acid sequence of a naturally occuring variant thereof; such that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to generate resistance against CGMMV in said plant.
 24. Method according to claim 21 or 22, in which the polynucleotide sequence encodes a protein or polypeptide that comprises, and preferably consist of: an amino acid sequence corresponding to a truncated part of the sequence given in SEQ ID no.2, to a Located ant of the sequence given in SEQ ID no.18 and/or to a truncated variant of the amino add sequence of a naturally occur variant thereof; an amino acid sequence corresponding to a truncated variant of the sequence given in SEQ ID no.6, to a truncated variant of the sequence given in SEQ M no.22 and/or to a truncated variant of the amino acid sequence of a naturally occuring variant thereof; an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no 20, and/or to the amino acid sequence of a naturally occuring variant &=of; such that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to generate resistance against CGMMV in said plant.
 25. Method according to claim 24, in which the polynucleotide sequence encodes a protein or polypeptide that comprises, and preferably consists of, the amino acid sequence given in SEQ ID no.2, the amino acid sequence given in SEQ ID no 18 and/or the amino acid sequence of a naturally occuring variant thereof, that has been truncated in the GDD-motif or in the P-loop.
 26. Method according to any of the preceding claims 18-25, further comprising at least one step of cultivating tile transformed plant cell into a mature plant.
 27. Method according to any of the preceding claims 18-25, fiber comprising at least one step of sexually or asexually reproducing or multiplying the transformed plant and/or the mature plant obtained from the transformed plant cell of claim
 26. 28. Method according to any of the preceding claims 18-25, in which the plant is a plant that is susceptible to infection with CGMMV, more preferably a plant belonging to the Cucurbitaceae family, such as melon (Cucumis melo), cucumber (C. sativus), watermelon (Citrullus vulgaris) and bottlegourd (Lagenaria siceraria).
 29. Genetic construct suitable for transforming a plant, said construct at least comprising nucleotide sequence that upon (at least) transformation into a plant and transcription into RNA generates resistance fragment infection with CGMMV in said plant, and, upon (at leas) transformation into a plant and transcription into RNA does not lead to generation of (any) replicase activity in said plant, and optionally comprising further elements of genetic constructs known per se.
 30. Genetic construct according to claim 29, at least comprising a nucleotide sequence that comprises, and preferably consists of: a nucleotide sequence corresponding to the sequence given in SEQ D no.1, to the sequence given in SEQ ID no.17 or to the nucleotide sequence of a naturally occuring variant thereof, in which—compared to the sequence of SEQ ID no.1, SEQ ID no. 17 and/or the ally occuring variant thereof—one or more nucleotides have been added, replaced and/or removed; a nucleotide sequence corresponding to the sequence given in SEQ ID no.5, to the sequence given in SEQ ID no,21, to the nucleotide sequence of a naturally occuring variant thereof, in which—compared to the sequence of SEQ ID no.5, SEQ ID no. 21 and/or the naturally occuring variant thereof—one or more nucleotides have been added replaced and/or removed; a nucleotide sequence corresponding to the sequence given in SEQ ID no.3, to the sequence given in SEQ ID no.19 or to the nucleotide sequence naturally occuring variant thereof; a nucleotide sequence corresponding to the sequence given in SEQ ID no.3, to the sequence given in SEQ ID no.19 or to the nucleotide sequence of a naturally occuring variant thereof in which—compared to the sequence of SEQ ID no.3, SEQ ID no. 19 and/or the naturally occuring variant thereof—one or more nucleotides have been added, replaced and/or removed; such that said construct is capable, upon (at least) transformation into a plant and transcription into RNA, to confer to said plant resistance against injection with CGMMV, and such that said construct, upon (at least) transformation into a plant and transcription into RNA, is not capable of generating of (any) replicase activity in said plant.
 31. Genetic construct according to claim 29 or 30, at least comprising a nucleotide sequence that encodes a polypeptide or protein that upon being expressed in a plant is capable of generating resistance against CGMMV in said plant; and upon being expressed in a plant has no replicase activity.
 32. Genetic construct according to claim 14, in which the nucleotide sequence encodes a protein or polypeptide that comprises, and preferably consists of: an amino acid sequence corresponding to the sequence given in SEQ ID no2, to the sequence given in SEQ ID no.18 or to the amino acid sequence of a naturally occuring variant thereof, in which—compared to the sequence of SEQ ID no.2, SEQ ID no.18 and/or the naturally occuring variant thereof—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed; an amino acid sequence corresponding to the sequence given in SEQ ID no.6, to the sequence given in SEQ ID no.22 or to the amino acid sequence of a naturally occuring variant thereof in which—compared to the sequence of SEQ ID no.6, SEQ ID no. 22 and/or the naturally occurring variant thereof—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no.20 or to the amino acid sequence of a naturally occurring variant thereof; an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no.20 or to the no acid sequence of a naturally occurring variant thereof, in which—compared to the sequence of SEQ ID no.4, SEQ ID no. 20 and/or the ray o f variant thereof—one or more amino acids have been added, replaced or removed, preferably replaced or removed, more preferably removed; or any combination thereof provided that the resulting protein or polypeptide shows no replicase activity, but is sill capable—upon expression in a plant—to generate resistance against CGMMV in said plant.
 33. Genetic construct according to claim 31 or 32, in which the nucleotide sequence encodes a protein or polypeptide that comprises, and preferably consists of: an amino acid sequence corresponding to a part or fragment of the sequence given in SEQ ID no.2, to a part or fragment of the sequence given in SEQ ID no.18 and/or to a part of Bent of the amino acid sequence of a naturally occuring variant thereof, or corresponding to a combination of two or more such parts or fragments; an amino acid sequence corresponding to a part or fragment of the sequence given in SEQ ID no.6, to a part or fragment of the sequence given in SEQ ID no.22 and/or to a part of fragment of the amino acid sequence of a naturally occuring variant thereof or corresponding to a combination of two or more such parts or fragments; an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no.20, and/or to the Amino acid sequence of a naturally occuring variant thereof; such that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to gene resistance against CGMMV in said plant.
 34. Genetic construct according to any of claim 31-33, in which the nucleotide sequence encodes a protein or polypeptide that comprises, and preferably consists of: an amino acid sequence corresponding to a truncated variant of the sequence given in SEQ ID no.2, to a truncated variant of the sequence given in SEQ ID no.18 and/or to a truncated variant of the amino acid sequence of a naturally occuring variant thereof, an amino acid sequence corresponding to a truncated variant of the sequence given in SEQ ID no.6, to a truncated variant of the sequence given in SEQ D no.22 and/or to a truncated variant of the amino acid sequence of a naturally occuring variant thereof; an amino acid sequence corresponding to the sequence given in SEQ ID no.4, to the sequence given in SEQ ID no 20, and/or to the amino acid sequence of a naturally occurring variant thereof; such that the resulting protein or polypeptide shows no replicase activity, but is still capable—upon expression in a plant—to generate resistance against CGMMV in said plant.
 35. Genetic construct according to claim 34, in which the nucleotide sequence encodes a protein or polypeptide that comprises, and preferably consists of the amino acid sequence given in SEQ ID no.2, the amino acid sequence given in SEQ ID no.18 and/or the amino acid sequence of a naturally occuring vacant thereof, that has been truncated in the GDD-motif or in the P-loop.
 36. Genetic construct according to any of claim 29-35, in which tie nucleotide sequence is under control of the plastocyanine-promoter.
 37. Genetic construct according to any of claims 29-36, in which the nucleotide sequence is preceded by the native CGMMV leader (5′-UTR) sequence.
 38. Genetic construct according to any of claims 29-37, in a form that can be stably maintained or inherited in a micro-organism, in particular a bacterium, more in particular a bacterium that can be used to transform a plant or plant material, such as Agrobacterium.
 39. Micro-organism, in particular bacterium, more in partcular a bacterium that can be used to transform a plant, such as Agrobacterium, that contains a genetic construct according to any of claims 29-38, and in particular according to claim
 38. 40. Transgenic plant or plant cell, obtainable or obtained by a method according to one of claims 29-38, or a descendant of such a plant.
 41. Plant, plant cell or plant material that has been transformed with genetic construct according to any of claims 29-38, or a descendant of such a plant.
 42. Plant according to claim 40 or 41, being a plant that is susceptible to infection with CGMMV, more preferably a plant belonging to the Cucurbitaceae family, such as melon (Cucumis melo), cucumber (C. sativus), watermelon (Citrullus vulgaris) and bottlegourd (Lagenaria siceraria)
 43. Cultivation material such as seed, tubers, roots, stat, seedlings for a plant according to claim 40, 41 or
 42. 